Canonical Allele Identifier: CA1619167101
Gene: HCP5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463830A= , CM000668.2:g.31463830A= GRCh38
NC_000006.11:g.31431607A= , CM000668.1:g.31431607A= GRCh37
NC_000006.10:g.31539586A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040662.1:n.560A=