Canonical Allele Identifier: CA449651434
Gene: HCP5 HGNC NCBI

Linked Data

gnomAD v4: 6-31464243-A-G
MyVariant Identifiers: chr6:g.31432020A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31464243A>G , CM000668.2:g.31464243A>G GRCh38
NC_000006.11:g.31432020A>G , CM000668.1:g.31432020A>G GRCh37
NC_000006.10:g.31539999A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.973A>G