Canonical Allele Identifier: CA449650611
Gene: HCP5 HGNC NCBI

Linked Data

dbSNP Id: rs1762865333
gnomAD v3: 6-31464091-G-A
gnomAD v4: 6-31464091-G-A
MyVariant Identifiers: chr6:g.31431868G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31464091G>A , CM000668.2:g.31464091G>A GRCh38
NC_000006.11:g.31431868G>A , CM000668.1:g.31431868G>A GRCh37
NC_000006.10:g.31539847G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.821G>A