Canonical Allele Identifier: CA449648522
Gene: HCP5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31431311C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31463534C>G , CM000668.2:g.31463534C>G GRCh38
NC_000006.11:g.31431311C>G , CM000668.1:g.31431311C>G GRCh37
NC_000006.10:g.31539290C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.264C>G