Canonical Allele Identifier: CA449650117
Gene: HCP5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31431706T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463929T>G , CM000668.2:g.31463929T>G GRCh38
NC_000006.11:g.31431706T>G , CM000668.1:g.31431706T>G GRCh37
NC_000006.10:g.31539685T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040662.1:n.659T>G