Canonical Allele Identifier: CA1358881712
Gene:

Genomic Alleles

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

Transcript Alleles

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