Canonical Allele Identifier: CA2695456276
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs2101522028

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17027888G>C , CM000663.2:g.17027888G>C GRCh38
NC_000001.10:g.17354383G>C , CM000663.1:g.17354383G>C GRCh37
NC_000001.9:g.17226970G>C NCBI36
NG_012340.1:g.31283C>G , LRG_316:g.31283C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.253-23C>G ENSP00000481376.2:n.253-23C>G
ENST00000491274.6:c.382-23C>G ENSP00000480482.2:n.382-23C>G
ENST00000375499.8:c.424-23C>G MANE Select ENSP00000364649.3:n.424-23C>G
ENST00000375499.7:c.424-23C>G ENSP00000364649.3:n.424-23C>G
ENST00000463045.2:c.253-23C>G ENSP00000481376.1:n.253-23C>G
ENST00000475506.1:n.341-23C>G
ENST00000485515.5:n.358-23C>G
ENST00000491274.5:c.382-23C>G ENSP00000480482.1:n.382-23C>G
NM_003000.2:c.424-23C>G , LRG_316t1:c.424-23C>G NP_002991.2:n.424-23C>G
NM_003000.3:c.424-23C>G MANE Select NP_002991.2:n.424-23C>G