Canonical Allele Identifier: CA1358881709
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.39263210G= , CM000665.2:g.39263210G= GRCh38
NC_000003.11:g.39304701G= , CM000665.1:g.39304701G= GRCh37
NC_000003.10:g.39279705G= NCBI36
NG_016362.1:g.23526C=

Transcript Alleles

HGVS Amino-acid change
XR_001740660.2:n.2727G=