Canonical Allele Identifier: CA1514272889
Gene:

Linked Data

dbSNP Id: rs6852435

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.174379628T>A , CM000666.2:g.174379628T>A GRCh38
NC_000004.11:g.175300779T>A , CM000666.1:g.175300779T>A GRCh37
NC_000004.10:g.175537354T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939487.1:n.842-8949T>A
XR_939488.1:n.211-8949T>A
XR_001741919.1:n.842-8949T>A
XR_001741920.1:n.211-8949T>A
XR_939487.2:n.842-8949T>A