Canonical Allele Identifier: CA449651425
Gene: HCP5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31432018T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31464241T>A , CM000668.2:g.31464241T>A GRCh38
NC_000006.11:g.31432018T>A , CM000668.1:g.31432018T>A GRCh37
NC_000006.10:g.31539997T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.971T>A