Canonical Allele Identifier: CA449649948

Gene: HCP5

Linked Data

• dbSNP Id: rs1762852811
• gnomAD v3: 6-31463869-A-T
• gnomAD v4: 6-31463869-A-T
• MyVariant Identifiers: chr6:g.31431646A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31463869A>T , CM000668.2:g.31463869A>T	GRCh38
NC_000006.11:g.31431646A>T , CM000668.1:g.31431646A>T	GRCh37
NC_000006.10:g.31539625A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.599A>T