Canonical Allele Identifier: CA1481405456
Gene:

Linked Data

dbSNP Id: rs1738872646

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102499643A>G , CM000666.2:g.102499643A>G GRCh38
NC_000004.11:g.103420800A>G , CM000666.1:g.103420800A>G GRCh37
NC_000004.10:g.103639832A>G NCBI36
NG_050628.1:g.3315A>G

Transcript Alleles

HGVS Amino-acid change
XM_011532467.1:c.643+1606T>C XP_011530769.1:n.643+1606T>C
NR_136202.1:n.48+2796T>C