Canonical Allele Identifier: CA1358881719
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.39263231A= , CM000665.2:g.39263231A= GRCh38
NC_000003.11:g.39304722A= , CM000665.1:g.39304722A= GRCh37
NC_000003.10:g.39279726A= NCBI36
NG_016362.1:g.23505T=

Transcript Alleles

HGVS Amino-acid change
XR_001740660.2:n.2748A=