Canonical Allele Identifier: CA1156080315
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs1557741248

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17028132A>G , CM000663.2:g.17028132A>G GRCh38
NC_000001.10:g.17354627A>G , CM000663.1:g.17354627A>G GRCh37
NC_000001.9:g.17227214A>G NCBI36
NG_012340.1:g.31039T>C , LRG_316:g.31039T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.253-267T>C ENSP00000481376.2:n.253-267T>C
ENST00000491274.6:c.382-267T>C ENSP00000480482.2:n.382-267T>C
ENST00000375499.8:c.424-267T>C MANE Select ENSP00000364649.3:n.424-267T>C
ENST00000375499.7:c.424-267T>C ENSP00000364649.3:n.424-267T>C
ENST00000463045.2:c.253-267T>C ENSP00000481376.1:n.253-267T>C
ENST00000475506.1:n.341-267T>C
ENST00000485515.5:n.358-267T>C
ENST00000491274.5:c.382-267T>C ENSP00000480482.1:n.382-267T>C
NM_003000.2:c.424-267T>C , LRG_316t1:c.424-267T>C NP_002991.2:n.424-267T>C
NM_003000.3:c.424-267T>C MANE Select NP_002991.2:n.424-267T>C