Canonical Allele Identifier: CA449649777

Gene: HCP5

Linked Data

• dbSNP Id: rs1273719227
• gnomAD v2: 6-31431586-A-T
• gnomAD v4: 6-31463809-A-T
• MyVariant Identifiers: chr6:g.31431586A>T (hg19) ; chr6:g.31463809A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31463809A>T , CM000668.2:g.31463809A>T	GRCh38
NC_000006.11:g.31431586A>T , CM000668.1:g.31431586A>T	GRCh37
NC_000006.10:g.31539565A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.539A>T