Canonical Allele Identifier: CA860367820
Gene:

Linked Data

dbSNP Id: rs1264389990

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129576721A>G , CM000671.2:g.129576721A>G GRCh38
NC_000009.11:g.132339000A>G , CM000671.1:g.132339000A>G GRCh37
NC_000009.10:g.131378821A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930390.1:n.182+1123A>G