Canonical Allele Identifier: CA3712431

Gene: HCP5

Linked Data

• dbSNP Id: rs766454183
• ExAC: 6:31431751 C / G
• gnomAD v2: 6-31431751-C-G
• gnomAD v4: 6-31463974-C-G
• MyVariant Identifiers: chr6:g.31431751C>G (hg19) ; chr6:g.31463974C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31463974C>G , CM000668.2:g.31463974C>G	GRCh38
NC_000006.11:g.31431751C>G , CM000668.1:g.31431751C>G	GRCh37
NC_000006.10:g.31539730C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.704C>G