Canonical Allele Identifier: CA1374121599
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.72266830A= , CM000665.2:g.72266830A= GRCh38
NC_000003.11:g.72315981A= , CM000665.1:g.72315981A= GRCh37
NC_000003.10:g.72398671A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940958.1:n.835+8278T=