Canonical Allele Identifier: CA6839534

Gene: HPD

Linked Data

• ClinVar Variation Id: 936109
• ClinVar RCV Id: RCV001204845
• dbSNP Id: rs755816788
• ExAC: 12:122284821 C / T
• gnomAD v2: 12-122284821-C-T
• gnomAD v3: 12-121846915-C-T
• gnomAD v4: 12-121846915-C-T
• COSMIC: COSM382797
• MyVariant Identifiers: chr12:g.122284821C>T (hg19) ; chr12:g.121846915C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121846915C>T , CM000674.2:g.121846915C>T	GRCh38
NC_000012.11:g.122284821C>T , CM000674.1:g.122284821C>T	GRCh37
NC_000012.10:g.120769204C>T	NCBI36
NG_016461.1:g.46697G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289004.8:c.778G>A MANE Select	ENSP00000289004.4:p.Gly260Arg
ENST00000543163.5:c.661G>A	ENSP00000441677.1:p.Gly221Arg
NM_001171993.1:c.661G>A	NP_001165464.1:p.Gly221Arg
NM_002150.2:c.778G>A	NP_002141.1:p.Gly260Arg
NM_002150.3:c.778G>A MANE Select	NP_002141.2:p.Gly260Arg
NM_001171993.2:c.661G>A	NP_001165464.1:p.Gly221Arg