Canonical Allele Identifier: CA449650099
Gene: HCP5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31431700A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463923A>G , CM000668.2:g.31463923A>G GRCh38
NC_000006.11:g.31431700A>G , CM000668.1:g.31431700A>G GRCh37
NC_000006.10:g.31539679A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040662.1:n.653A>G