Canonical Allele Identifier: CA1619167100
Gene: HCP5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463829A= , CM000668.2:g.31463829A= GRCh38
NC_000006.11:g.31431606A= , CM000668.1:g.31431606A= GRCh37
NC_000006.10:g.31539585A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040662.1:n.559A=