Canonical Allele Identifier: CA3712436

Gene: HCP5

Linked Data

• dbSNP Id: rs757113671
• ExAC: 6:31431783 C / A
• gnomAD v2: 6-31431783-C-A
• gnomAD v3: 6-31464006-C-A
• gnomAD v4: 6-31464006-C-A
• MyVariant Identifiers: chr6:g.31431783C>A (hg19) ; chr6:g.31464006C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31464006C>A , CM000668.2:g.31464006C>A	GRCh38
NC_000006.11:g.31431783C>A , CM000668.1:g.31431783C>A	GRCh37
NC_000006.10:g.31539762C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.736C>A