Canonical Allele Identifier: CA1619166969
Gene: HCP5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463383A= , CM000668.2:g.31463383A= GRCh38
NC_000006.11:g.31431160A= , CM000668.1:g.31431160A= GRCh37
NC_000006.10:g.31539139A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.113A=