Canonical Allele Identifier: CA1870932962
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.108092837T= , CM000671.2:g.108092837T= GRCh38
NC_000009.11:g.110855118T= , CM000671.1:g.110855118T= GRCh37
NC_000009.10:g.109894939T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930239.1:n.461-39543A=
XR_001746881.1:n.668-39543A=
XR_001746882.1:n.668-39543A=