Canonical Allele Identifier: CA2580060635

Gene: SDHB

Linked Data

• ClinVar Variation Id: 2134026
• ClinVar RCV Id: RCV003058031
• gnomAD v4: 1-17028745-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17028745G>A , CM000663.2:g.17028745G>A	GRCh38
NC_000001.10:g.17355240G>A , CM000663.1:g.17355240G>A	GRCh37
NC_000001.9:g.17227827G>A	NCBI36
NG_012340.1:g.30426C>T , LRG_316:g.30426C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.116-9C>T	ENSP00000481376.2:n.116-9C>T
ENST00000491274.6:c.245-9C>T	ENSP00000480482.2:n.245-9C>T
ENST00000375499.8:c.287-9C>T MANE Select	ENSP00000364649.3:n.287-9C>T
ENST00000375499.7:c.287-9C>T	ENSP00000364649.3:n.287-9C>T
ENST00000463045.2:c.116-9C>T	ENSP00000481376.1:n.116-9C>T
ENST00000475506.1:n.204-9C>T
ENST00000485515.5:n.275-9C>T
ENST00000491274.5:c.245-9C>T	ENSP00000480482.1:n.245-9C>T
NM_003000.2:c.287-9C>T , LRG_316t1:c.287-9C>T	NP_002991.2:n.287-9C>T
NM_003000.3:c.287-9C>T MANE Select	NP_002991.2:n.287-9C>T