Canonical Allele Identifier: CA1066140548
Gene:

Linked Data

dbSNP Id: rs1738893654

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102499962G>A , CM000666.2:g.102499962G>A GRCh38
NC_000004.11:g.103421119G>A , CM000666.1:g.103421119G>A GRCh37
NC_000004.10:g.103640151G>A NCBI36
NG_050628.1:g.3634G>A

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+1287C>T XP_011530769.1:n.643+1287C>T
NR_136202.1:n.48+2477C>T