Canonical Allele Identifier: CA449651882

Gene: HCP5

Linked Data

• dbSNP Id: rs1269318547
• gnomAD v2: 6-31432117-C-A
• gnomAD v3: 6-31464340-C-A
• gnomAD v4: 6-31464340-C-A
• MyVariant Identifiers: chr6:g.31432117C>A (hg19) ; chr6:g.31464340C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31464340C>A , CM000668.2:g.31464340C>A	GRCh38
NC_000006.11:g.31432117C>A , CM000668.1:g.31432117C>A	GRCh37
NC_000006.10:g.31540096C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.1070C>A