Canonical Allele Identifier: CA2766254559
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19932476C>A , CM000686.2:g.19932476C>A GRCh38
NC_000024.9:g.22094362C>A , CM000686.1:g.22094362C>A GRCh37
NC_000024.8:g.20553750C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000616477.1:n.25G>T