Canonical Allele Identifier: CA449650329
Gene: HCP5 HGNC NCBI

Linked Data

gnomAD v4: 6-31464006-C-T
MyVariant Identifiers: chr6:g.31431783C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31464006C>T , CM000668.2:g.31464006C>T GRCh38
NC_000006.11:g.31431783C>T , CM000668.1:g.31431783C>T GRCh37
NC_000006.10:g.31539762C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040662.1:n.736C>T