Canonical Allele Identifier: CA449650132

Gene: HCP5

Linked Data

• dbSNP Id: rs1280373891
• gnomAD v2: 6-31431712-T-A
• gnomAD v3: 6-31463935-T-A
• gnomAD v4: 6-31463935-T-A
• MyVariant Identifiers: chr6:g.31431712T>A (hg19) ; chr6:g.31463935T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31463935T>A , CM000668.2:g.31463935T>A	GRCh38
NC_000006.11:g.31431712T>A , CM000668.1:g.31431712T>A	GRCh37
NC_000006.10:g.31539691T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.665T>A