Canonical Allele Identifier: CA449650054
Gene: HCP5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31431685C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463908C>A , CM000668.2:g.31463908C>A GRCh38
NC_000006.11:g.31431685C>A , CM000668.1:g.31431685C>A GRCh37
NC_000006.10:g.31539664C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040662.1:n.638C>A