Canonical Allele Identifier: CA449650412
Gene: HCP5 HGNC NCBI

Linked Data

gnomAD v4: 6-31464034-T-C
MyVariant Identifiers: chr6:g.31431811T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31464034T>C , CM000668.2:g.31464034T>C GRCh38
NC_000006.11:g.31431811T>C , CM000668.1:g.31431811T>C GRCh37
NC_000006.10:g.31539790T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040662.1:n.764T>C