Canonical Allele Identifier: CA449648832
Gene: HCP5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31431413G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463636G>C , CM000668.2:g.31463636G>C GRCh38
NC_000006.11:g.31431413G>C , CM000668.1:g.31431413G>C GRCh37
NC_000006.10:g.31539392G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.366G>C