Canonical Allele Identifier: CA449651828
Gene: HCP5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31432107T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31464330T>A , CM000668.2:g.31464330T>A GRCh38
NC_000006.11:g.31432107T>A , CM000668.1:g.31432107T>A GRCh37
NC_000006.10:g.31540086T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.1060T>A