Canonical Allele Identifier: CA449652002

Gene: HCP5

Linked Data

• gnomAD v4: 6-31464362-T-A
• MyVariant Identifiers: chr6:g.31432139T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31464362T>A , CM000668.2:g.31464362T>A	GRCh38
NC_000006.11:g.31432139T>A , CM000668.1:g.31432139T>A	GRCh37
NC_000006.10:g.31540118T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.1092T>A