Canonical Allele Identifier: CA449650286
Gene: HCP5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31431768C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463991C>G , CM000668.2:g.31463991C>G GRCh38
NC_000006.11:g.31431768C>G , CM000668.1:g.31431768C>G GRCh37
NC_000006.10:g.31539747C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.721C>G