Canonical Allele Identifier: CA449650138
Gene: HCP5 HGNC NCBI

Linked Data

dbSNP Id: rs551035173
gnomAD v3: 6-31463937-C-G
gnomAD v4: 6-31463937-C-G
MyVariant Identifiers: chr6:g.31431714C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463937C>G , CM000668.2:g.31463937C>G GRCh38
NC_000006.11:g.31431714C>G , CM000668.1:g.31431714C>G GRCh37
NC_000006.10:g.31539693C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.667C>G