Canonical Allele Identifier: CA3712451

Gene: HCP5

Linked Data

• dbSNP Id: rs765599668
• ExAC: 6:31431896 A / C
• gnomAD v2: 6-31431896-A-C
• MyVariant Identifiers: chr6:g.31431896A>C (hg19) ; chr6:g.31464119A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31464119A>C , CM000668.2:g.31464119A>C	GRCh38
NC_000006.11:g.31431896A>C , CM000668.1:g.31431896A>C	GRCh37
NC_000006.10:g.31539875A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.849A>C