Canonical Allele Identifier: CA449650335
Gene: HCP5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31431785G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31464008G>C , CM000668.2:g.31464008G>C GRCh38
NC_000006.11:g.31431785G>C , CM000668.1:g.31431785G>C GRCh37
NC_000006.10:g.31539764G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040662.1:n.738G>C