Canonical Allele Identifier: CA136868368

Gene: HCP5

Linked Data

• dbSNP Id: rs79999641
• gnomAD v4: 6-31463548-T-C
• MyVariant Identifiers: chr6:g.31431325T>C (hg19) ; chr6:g.31463548T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31463548T>C , CM000668.2:g.31463548T>C	GRCh38
NC_000006.11:g.31431325T>C , CM000668.1:g.31431325T>C	GRCh37
NC_000006.10:g.31539304T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.278T>C