Canonical Allele Identifier: CA136868344

Gene: HCP5

Linked Data

• dbSNP Id: rs936949676
• MyVariant Identifiers: chr6:g.31431231C>T (hg19) ; chr6:g.31463454C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31463454C>T , CM000668.2:g.31463454C>T	GRCh38
NC_000006.11:g.31431231C>T , CM000668.1:g.31431231C>T	GRCh37
NC_000006.10:g.31539210C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.184C>T