Canonical Allele Identifier: CA449650080
Gene: HCP5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31431694A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463917A>C , CM000668.2:g.31463917A>C GRCh38
NC_000006.11:g.31431694A>C , CM000668.1:g.31431694A>C GRCh37
NC_000006.10:g.31539673A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040662.1:n.647A>C