Canonical Allele Identifier: CA338272980

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17354318A>C (hg19) ; chr1:g.17027823A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027823A>C , CM000663.2:g.17027823A>C	GRCh38
NC_000001.10:g.17354318A>C , CM000663.1:g.17354318A>C	GRCh37
NC_000001.9:g.17226905A>C	NCBI36
NG_012340.1:g.31348T>G , LRG_316:g.31348T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.295T>G	ENSP00000481376.2:p.Tyr99Asp
ENST00000491274.6:c.424T>G	ENSP00000480482.2:p.Tyr142Asp
ENST00000375499.8:c.466T>G MANE Select	ENSP00000364649.3:p.Tyr156Asp
ENST00000375499.7:c.466T>G	ENSP00000364649.3:p.Tyr156Asp
ENST00000463045.2:c.295T>G	ENSP00000481376.1:p.Tyr99Asp
ENST00000475506.1:n.383T>G
ENST00000485515.5:n.400T>G
ENST00000491274.5:c.424T>G	ENSP00000480482.1:p.Tyr142Asp
NM_003000.2:c.466T>G , LRG_316t1:c.466T>G	NP_002991.2:p.Tyr156Asp
NM_003000.3:c.466T>G MANE Select	NP_002991.2:p.Tyr156Asp