Canonical Allele Identifier: CA1358881714
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.39263227C= , CM000665.2:g.39263227C= GRCh38
NC_000003.11:g.39304718C= , CM000665.1:g.39304718C= GRCh37
NC_000003.10:g.39279722C= NCBI36
NG_016362.1:g.23509G=

Transcript Alleles

HGVS Amino-acid change
XR_001740660.2:n.2744C=