Allele Registry

WARNING - Protein Allele ID and Protein Sequence HGVS API Requests Temporarily Disabled:
We are investigating the periodic unresponsiveness in the Registry.
Although replication attempts were unsuccessful, there is a high correlation with protein alleles. And with haplotype HGVS queries.
This temporarily affects the API and the UI.

ClinGen Allele Registry

Canonical Allele Identifier: CA10581751

Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 239422

ClinVar RCV Id: RCV000234165

dbSNP Id: rs878854573

MyVariant Identifiers: chr1:g.17371301G>T (hg19) chr1:g.17044806G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17044806G>T , CM000663.2:g.17044806G>T	GRCh38
NC_000001.10:g.17371301G>T , CM000663.1:g.17371301G>T	GRCh37
NC_000001.9:g.17243888G>T	NCBI36
NG_012340.1:g.14365C>A , LRG_316:g.14365C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.-17C>A	ENSP00000481376.2:n.-17C>A
ENST00000491274.6:c.113C>A	ENSP00000480482.2:p.Ala38Asp
ENST00000375499.8:c.155C>A MANE Select	ENSP00000364649.3:p.Ala52Asp
ENST00000375499.7:c.155C>A	ENSP00000364649.3:p.Ala52Asp
ENST00000463045.2:c.-17C>A	ENSP00000481376.1:n.-17C>A
ENST00000466613.2:n.167C>A
ENST00000475506.1:n.72C>A
ENST00000485515.5:n.143C>A
ENST00000491274.5:c.113C>A	ENSP00000480482.1:p.Ala38Asp
NM_003000.2:c.155C>A , LRG_316t1:c.155C>A	NP_002991.2:p.Ala52Asp
NM_003000.3:c.155C>A MANE Select	NP_002991.2:p.Ala52Asp