Canonical Allele Identifier: CA1644769189
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.87942862T>A , CM000668.2:g.87942862T>A GRCh38
NC_000006.11:g.88652580T>A , CM000668.1:g.88652580T>A GRCh37
NC_000006.10:g.88709299T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001744246.1:n.1581T>A