Canonical Allele Identifier: CA136868792

Gene: HCP5

Linked Data

• dbSNP Id: rs897909193
• gnomAD v4: 6-31464335-A-T
• MyVariant Identifiers: chr6:g.31432112A>T (hg19) ; chr6:g.31464335A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31464335A>T , CM000668.2:g.31464335A>T	GRCh38
NC_000006.11:g.31432112A>T , CM000668.1:g.31432112A>T	GRCh37
NC_000006.10:g.31540091A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.1065A>T