Canonical Allele Identifier: CA1481405416
Gene:

Linked Data

dbSNP Id: rs1738870848

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102499608T>C , CM000666.2:g.102499608T>C GRCh38
NC_000004.11:g.103420765T>C , CM000666.1:g.103420765T>C GRCh37
NC_000004.10:g.103639797T>C NCBI36
NG_050628.1:g.3280T>C

Transcript Alleles

HGVS Amino-acid change
XM_011532467.1:c.643+1641A>G XP_011530769.1:n.643+1641A>G
NR_136202.1:n.48+2831A>G