Canonical Allele Identifier: CA2766254562
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19932486T>C , CM000686.2:g.19932486T>C GRCh38
NC_000024.9:g.22094372T>C , CM000686.1:g.22094372T>C GRCh37
NC_000024.8:g.20553760T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000616477.1:n.15A>G