Canonical Allele Identifier: CA449649463
Gene: HCP5 HGNC NCBI

Linked Data

gnomAD v4: 6-31463743-C-A
MyVariant Identifiers: chr6:g.31431520C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463743C>A , CM000668.2:g.31463743C>A GRCh38
NC_000006.11:g.31431520C>A , CM000668.1:g.31431520C>A GRCh37
NC_000006.10:g.31539499C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.473C>A