Canonical Allele Identifier: CA449650362

Gene: HCP5

Linked Data

• dbSNP Id: rs1481036167
• gnomAD v2: 6-31431795-G-A
• gnomAD v4: 6-31464018-G-A
• MyVariant Identifiers: chr6:g.31431795G>A (hg19) ; chr6:g.31464018G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31464018G>A , CM000668.2:g.31464018G>A	GRCh38
NC_000006.11:g.31431795G>A , CM000668.1:g.31431795G>A	GRCh37
NC_000006.10:g.31539774G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_040662.1:n.748G>A