Canonical Allele Identifier: CA449649466
Gene: HCP5 HGNC NCBI

Linked Data

dbSNP Id: rs1762844493
MyVariant Identifiers: chr6:g.31431520C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463743C>G , CM000668.2:g.31463743C>G GRCh38
NC_000006.11:g.31431520C>G , CM000668.1:g.31431520C>G GRCh37
NC_000006.10:g.31539499C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.473C>G