Canonical Allele Identifier: CA449651358

Gene: HCP5

Linked Data

• gnomAD v4: 6-31464222-T-C
• MyVariant Identifiers: chr6:g.31431999T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31464222T>C , CM000668.2:g.31464222T>C	GRCh38
NC_000006.11:g.31431999T>C , CM000668.1:g.31431999T>C	GRCh37
NC_000006.10:g.31539978T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.952T>C