Canonical Allele Identifier: CA1880834366
Gene:

Linked Data

dbSNP Id: rs1564321340

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129576828T>A , CM000671.2:g.129576828T>A GRCh38
NC_000009.11:g.132339107T>A , CM000671.1:g.132339107T>A GRCh37
NC_000009.10:g.131378928T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930390.1:n.182+1230T>A