Canonical Allele Identifier: CA1619167001
Gene: HCP5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463537T= , CM000668.2:g.31463537T= GRCh38
NC_000006.11:g.31431314T= , CM000668.1:g.31431314T= GRCh37
NC_000006.10:g.31539293T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.267T=