Canonical Allele Identifier: CA449649844
Gene: HCP5 HGNC NCBI

Linked Data

gnomAD v4: 6-31463831-C-A
MyVariant Identifiers: chr6:g.31431608C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463831C>A , CM000668.2:g.31463831C>A GRCh38
NC_000006.11:g.31431608C>A , CM000668.1:g.31431608C>A GRCh37
NC_000006.10:g.31539587C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040662.1:n.561C>A