Canonical Allele Identifier: CA449649385
Gene: HCP5 HGNC NCBI

Linked Data

gnomAD v4: 6-31463729-C-A
MyVariant Identifiers: chr6:g.31431506C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463729C>A , CM000668.2:g.31463729C>A GRCh38
NC_000006.11:g.31431506C>A , CM000668.1:g.31431506C>A GRCh37
NC_000006.10:g.31539485C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.459C>A