Canonical Allele Identifier: CA338272596

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17354276A>C (hg19) ; chr1:g.17027781A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027781A>C , CM000663.2:g.17027781A>C	GRCh38
NC_000001.10:g.17354276A>C , CM000663.1:g.17354276A>C	GRCh37
NC_000001.9:g.17226863A>C	NCBI36
NG_012340.1:g.31390T>G , LRG_316:g.31390T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.337T>G	ENSP00000481376.2:p.Tyr113Asp
ENST00000491274.6:c.466T>G	ENSP00000480482.2:p.Tyr156Asp
ENST00000375499.8:c.508T>G MANE Select	ENSP00000364649.3:p.Tyr170Asp
ENST00000375499.7:c.508T>G	ENSP00000364649.3:p.Tyr170Asp
ENST00000463045.2:c.337T>G	ENSP00000481376.1:p.Tyr113Asp
ENST00000475506.1:n.425T>G
ENST00000485515.5:n.442T>G
ENST00000491274.5:c.466T>G	ENSP00000480482.1:p.Tyr156Asp
NM_003000.2:c.508T>G , LRG_316t1:c.508T>G	NP_002991.2:p.Tyr170Asp
NM_003000.3:c.508T>G MANE Select	NP_002991.2:p.Tyr170Asp