Canonical Allele Identifier: CA1859751114
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.82696232C>A , CM000671.2:g.82696232C>A GRCh38
NC_000009.11:g.85311147C>A , CM000671.1:g.85311147C>A GRCh37
NC_000009.10:g.84500967C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000637606.1:n.986-83647C>A
XR_001746782.1:n.242-83647C>A