Canonical Allele Identifier: CA338272960
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs1557741131
gnomAD v4: 1-17027823-A-G

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.295T>C ENSP00000481376.2:p.Tyr99His
ENST00000491274.6:c.424T>C ENSP00000480482.2:p.Tyr142His
ENST00000375499.8:c.466T>C MANE Select ENSP00000364649.3:p.Tyr156His
ENST00000375499.7:c.466T>C ENSP00000364649.3:p.Tyr156His
ENST00000463045.2:c.295T>C ENSP00000481376.1:p.Tyr99His
ENST00000475506.1:n.383T>C
ENST00000485515.5:n.400T>C
ENST00000491274.5:c.424T>C ENSP00000480482.1:p.Tyr142His
NM_003000.2:c.466T>C , LRG_316t1:c.466T>C NP_002991.2:p.Tyr156His
NM_003000.3:c.466T>C MANE Select NP_002991.2:p.Tyr156His