Canonical Allele Identifier: CA1839056762
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21756116A= , CM000671.2:g.21756116A= GRCh38
NC_000009.11:g.21756115A= , CM000671.1:g.21756115A= GRCh37
NC_000009.10:g.21746115A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746563.2:n.163+11709T=