Canonical Allele Identifier: CA1358881713
Gene:

Linked Data

dbSNP Id: rs561471503

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.39263216C>T , CM000665.2:g.39263216C>T GRCh38
NC_000003.11:g.39304707C>T , CM000665.1:g.39304707C>T GRCh37
NC_000003.10:g.39279711C>T NCBI36
NG_016362.1:g.23520G>A

Transcript Alleles

HGVS Amino-acid change
XR_001740660.2:n.2733C>T