Canonical Allele Identifier: CA449649761

Gene: HCP5

Linked Data

• dbSNP Id: rs1323777669
• gnomAD v2: 6-31431580-C-T
• gnomAD v4: 6-31463803-C-T
• MyVariant Identifiers: chr6:g.31431580C>T (hg19) ; chr6:g.31463803C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31463803C>T , CM000668.2:g.31463803C>T	GRCh38
NC_000006.11:g.31431580C>T , CM000668.1:g.31431580C>T	GRCh37
NC_000006.10:g.31539559C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.533C>T