Canonical Allele Identifier: CA2501517100
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31440108C>A , CM000668.2:g.31440108C>A GRCh38
NC_000006.11:g.31407885C>A , CM000668.1:g.31407885C>A GRCh37
NC_000006.10:g.31515864C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926694.1:n.55-56G>T