Canonical Allele Identifier: CA449648352
Gene: HCP5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31431255G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463478G>A , CM000668.2:g.31463478G>A GRCh38
NC_000006.11:g.31431255G>A , CM000668.1:g.31431255G>A GRCh37
NC_000006.10:g.31539234G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.208G>A