Canonical Allele Identifier: CA1870932942
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.108092816A= , CM000671.2:g.108092816A= GRCh38
NC_000009.11:g.110855097A= , CM000671.1:g.110855097A= GRCh37
NC_000009.10:g.109894918A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930239.1:n.461-39522T=
XR_001746881.1:n.668-39522T=
XR_001746882.1:n.668-39522T=