Canonical Allele Identifier: CA1619166991
Gene: HCP5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463507A= , CM000668.2:g.31463507A= GRCh38
NC_000006.11:g.31431284A= , CM000668.1:g.31431284A= GRCh37
NC_000006.10:g.31539263A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.237A=