Canonical Allele Identifier: CA1156080336
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs2078002054
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17028178G>A , CM000663.2:g.17028178G>A GRCh38
NC_000001.10:g.17354673G>A , CM000663.1:g.17354673G>A GRCh37
NC_000001.9:g.17227260G>A NCBI36
NG_012340.1:g.30993C>T , LRG_316:g.30993C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.253-313C>T ENSP00000481376.2:n.253-313C>T
ENST00000491274.6:c.382-313C>T ENSP00000480482.2:n.382-313C>T
ENST00000375499.8:c.424-313C>T MANE Select ENSP00000364649.3:n.424-313C>T
ENST00000375499.7:c.424-313C>T ENSP00000364649.3:n.424-313C>T
ENST00000463045.2:c.253-313C>T ENSP00000481376.1:n.253-313C>T
ENST00000475506.1:n.341-313C>T
ENST00000485515.5:n.358-313C>T
ENST00000491274.5:c.382-313C>T ENSP00000480482.1:n.382-313C>T
NM_003000.2:c.424-313C>T , LRG_316t1:c.424-313C>T NP_002991.2:n.424-313C>T
NM_003000.3:c.424-313C>T MANE Select NP_002991.2:n.424-313C>T
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