Canonical Allele Identifier: CA449650341
Gene: HCP5 HGNC NCBI

Linked Data

gnomAD v4: 6-31464010-T-C
MyVariant Identifiers: chr6:g.31431787T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31464010T>C , CM000668.2:g.31464010T>C GRCh38
NC_000006.11:g.31431787T>C , CM000668.1:g.31431787T>C GRCh37
NC_000006.10:g.31539766T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040662.1:n.740T>C