Canonical Allele Identifier: CA136868349

Gene: HCP5

Linked Data

• dbSNP Id: rs991653861
• MyVariant Identifiers: chr6:g.31431234C>T (hg19) ; chr6:g.31463457C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31463457C>T , CM000668.2:g.31463457C>T	GRCh38
NC_000006.11:g.31431234C>T , CM000668.1:g.31431234C>T	GRCh37
NC_000006.10:g.31539213C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.187C>T