Canonical Allele Identifier: CA449650359
Gene: HCP5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31431793G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31464016G>T , CM000668.2:g.31464016G>T GRCh38
NC_000006.11:g.31431793G>T , CM000668.1:g.31431793G>T GRCh37
NC_000006.10:g.31539772G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040662.1:n.746G>T