Canonical Allele Identifier: CA449652025
Gene: HCP5 HGNC NCBI

Linked Data

gnomAD v4: 6-31464367-G-A
MyVariant Identifiers: chr6:g.31432144G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31464367G>A , CM000668.2:g.31464367G>A GRCh38
NC_000006.11:g.31432144G>A , CM000668.1:g.31432144G>A GRCh37
NC_000006.10:g.31540123G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.1097G>A