Canonical Allele Identifier: CA1870932992
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.108092887A= , CM000671.2:g.108092887A= GRCh38
NC_000009.11:g.110855168A= , CM000671.1:g.110855168A= GRCh37
NC_000009.10:g.109894989A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930239.1:n.461-39593T=
XR_001746881.1:n.668-39593T=
XR_001746882.1:n.668-39593T=