Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.37 (A)
Location

Chromosome 5:96766240 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 23 HGVS names - click the plus to show

5:g.96766240A>G
ENST00000508608.2:c.2019+95A>G
ENST00000511049.2:c.1836+95A>G
ENST00000395813.2:c.1881+95A>G
ENST00000508579.2:c.1026+95A>G
ENST00000484552.2:c.1105+95A>G
ENST00000508830.2:c.2130+95A>G
ENST00000325674.8:c.1047+95A>G
ENST00000510756.2:c.2064+95A>G
ENST00000296754.4:c.2819-3012T>C
ENST00000511782.2:c.1839+95A>G
ENST00000510156.2:c.1881+95A>G
ENST00000395812.3:c.2007+95A>G
ENST00000509903.2:c.1776+95A>G
ENST00000309190.6:c.1815+95A>G
ENST00000341926.4:c.1881+95A>G
ENST00000510098.1:c.366+95A>G
ENST00000510500.2:c.1150+95A>G
ENST00000338252.4:c.1842+95A>G
ENST00000437034.3:c.1136+95A>G
ENST00000348386.4:n.1823+95A>G
ENST00000515663.2:c.1050+95A>G
ENST00000504465.2:c.1665+95A>G

This variation has assays on 9 chips - click the plus to show

Variation displays