Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.44 (C)
Location

Chromosome 7:34742415 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 16 HGVS names - click the plus to show

7:g.34742415C>T
ENST00000419766.2:n.162-13599G>A
ENST00000359791.2:c.281-36047C>T
ENST00000381544.3:c.280+57731C>T
ENST00000436945.4:n.268-13599G>A
ENST00000531252.2:c.281-36080C>T
ENST00000431669.2:n.165-13599G>A
ENST00000381539.3:c.281-36047C>T
ENST00000381553.4:c.281-36047C>T
ENST00000396095.3:c.281-36047C>T
ENST00000381542.2:c.280+57731C>T
ENST00000439852.2:n.200-13599G>A
ENST00000428922.2:n.81-13599G>A
ENST00000539747.2:n.81-13599G>A
ENST00000358772.5:n.200-13599G>A
ENST00000360581.2:c.281-36047C>T

Variation displays