Canonical Allele Identifier: CA449651768
Gene: HCP5 HGNC NCBI

Linked Data

dbSNP Id: rs1762875830
gnomAD v4: 6-31464319-A-G
MyVariant Identifiers: chr6:g.31432096A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31464319A>G , CM000668.2:g.31464319A>G GRCh38
NC_000006.11:g.31432096A>G , CM000668.1:g.31432096A>G GRCh37
NC_000006.10:g.31540075A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.1049A>G