Canonical Allele Identifier: CA1066140436
Gene:

Linked Data

dbSNP Id: rs1183511416

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102499787A>G , CM000666.2:g.102499787A>G GRCh38
NC_000004.11:g.103420944A>G , CM000666.1:g.103420944A>G GRCh37
NC_000004.10:g.103639976A>G NCBI36
NG_050628.1:g.3459A>G

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+1462T>C XP_011530769.1:n.643+1462T>C
NR_136202.1:n.48+2652T>C