Canonical Allele Identifier: CA1481405730
Gene:

Linked Data

dbSNP Id: rs573380365

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102499809C>A , CM000666.2:g.102499809C>A GRCh38
NC_000004.11:g.103420966C>A , CM000666.1:g.103420966C>A GRCh37
NC_000004.10:g.103639998C>A NCBI36
NG_050628.1:g.3481C>A

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+1440G>T XP_011530769.1:n.643+1440G>T
NR_136202.1:n.48+2630G>T