Canonical Allele Identifier: CA1066140550
Gene:

Linked Data

dbSNP Id: rs1738893798

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102499966G>A , CM000666.2:g.102499966G>A GRCh38
NC_000004.11:g.103421123G>A , CM000666.1:g.103421123G>A GRCh37
NC_000004.10:g.103640155G>A NCBI36
NG_050628.1:g.3638G>A

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+1283C>T XP_011530769.1:n.643+1283C>T
NR_136202.1:n.48+2473C>T