Original source

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

Alleles
C/T | Ambiguity code: Y | MAF: 0.13 (T)
Location

Chromosome 5:96786506 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 4 synonyms - click the plus to show

This variation has 7 HGVS names - click the plus to show

5:g.96786506C>T
ENST00000443439.4:c.1723G>A
ENSP00000406304.2:p.Asp575Asn
ENST00000507859.1:n.386G>A
ENST00000514604.3:n.147G>A
ENST00000296754.5:c.1723G>A
ENSP00000296754.3:p.Asp575Asn

This variation has assays on 13 chips - click the plus to show

Variation displays