Canonical Allele Identifier: CA821226179
Gene:

Linked Data

dbSNP Id: rs1270780605

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155817523T>A , CM000668.2:g.155817523T>A GRCh38
NC_000006.11:g.156138657T>A , CM000668.1:g.156138657T>A GRCh37
NC_000006.10:g.156180349T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943142.1:n.79+24104T>A
XR_943146.1:n.552-2853A>T
XR_001744423.1:n.606-2853A>T
XR_001744424.1:n.79+24104T>A