Canonical Allele Identifier: CA2580060652

Gene: SDHB

Linked Data

• ClinVar Variation Id: 2027010
• ClinVar RCV Id: RCV002871650

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17044743T>A , CM000663.2:g.17044743T>A	GRCh38
NC_000001.10:g.17371238T>A , CM000663.1:g.17371238T>A	GRCh37
NC_000001.9:g.17243825T>A	NCBI36
NG_012340.1:g.14428A>T , LRG_316:g.14428A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.29+18A>T	ENSP00000481376.2:n.29+18A>T
ENST00000491274.6:c.158+18A>T	ENSP00000480482.2:n.158+18A>T
ENST00000375499.8:c.200+18A>T MANE Select	ENSP00000364649.3:n.200+18A>T
ENST00000375499.7:c.200+18A>T	ENSP00000364649.3:n.200+18A>T
ENST00000463045.2:c.29+18A>T	ENSP00000481376.1:n.29+18A>T
ENST00000466613.2:n.212+18A>T
ENST00000475506.1:n.117+18A>T
ENST00000485515.5:n.188+18A>T
ENST00000491274.5:c.158+18A>T	ENSP00000480482.1:n.158+18A>T
NM_003000.2:c.200+18A>T , LRG_316t1:c.200+18A>T	NP_002991.2:n.200+18A>T
NM_003000.3:c.200+18A>T MANE Select	NP_002991.2:n.200+18A>T