Canonical Allele Identifier: CA1619166978
Gene: HCP5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463421T= , CM000668.2:g.31463421T= GRCh38
NC_000006.11:g.31431198T= , CM000668.1:g.31431198T= GRCh37
NC_000006.10:g.31539177T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.151T=