Canonical Allele Identifier: CA3712426

Gene: HCP5

Linked Data

• dbSNP Id: rs774796867
• ExAC: 6:31431729 A / T
• gnomAD v2: 6-31431729-A-T
• gnomAD v4: 6-31463952-A-T
• MyVariant Identifiers: chr6:g.31431729A>T (hg19) ; chr6:g.31431729_31431732delinsTCTC (hg19) ; chr6:g.31463952A>T (hg38) ; chr6:g.31463952_31463955delinsTCTC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31463952A>T , CM000668.2:g.31463952A>T	GRCh38
NC_000006.11:g.31431729A>T , CM000668.1:g.31431729A>T	GRCh37
NC_000006.10:g.31539708A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.682A>T