Canonical Allele Identifier: CA136868357

Gene: HCP5

Linked Data

• dbSNP Id: rs904094559
• gnomAD v3: 6-31463519-G-A
• gnomAD v4: 6-31463519-G-A
• MyVariant Identifiers: chr6:g.31431296G>A (hg19) ; chr6:g.31463519G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31463519G>A , CM000668.2:g.31463519G>A	GRCh38
NC_000006.11:g.31431296G>A , CM000668.1:g.31431296G>A	GRCh37
NC_000006.10:g.31539275G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.249G>A