Canonical Allele Identifier: CA449648070

Gene: HCP5

Linked Data

• dbSNP Id: rs1762830542
• gnomAD v4: 6-31463382-A-G
• MyVariant Identifiers: chr6:g.31431159A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31463382A>G , CM000668.2:g.31463382A>G	GRCh38
NC_000006.11:g.31431159A>G , CM000668.1:g.31431159A>G	GRCh37
NC_000006.10:g.31539138A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.112A>G