Canonical Allele Identifier: CA1156080114
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs1570947781
gnomAD v4: 1-17027657-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17027657G>A , CM000663.2:g.17027657G>A GRCh38
NC_000001.10:g.17354152G>A , CM000663.1:g.17354152G>A GRCh37
NC_000001.9:g.17226739G>A NCBI36
NG_012340.1:g.31514C>T , LRG_316:g.31514C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.369+92C>T ENSP00000481376.2:n.369+92C>T
ENST00000491274.6:c.498+92C>T ENSP00000480482.2:n.498+92C>T
ENST00000375499.8:c.540+92C>T MANE Select ENSP00000364649.3:n.540+92C>T
ENST00000375499.7:c.540+92C>T ENSP00000364649.3:n.540+92C>T
ENST00000475506.1:n.549C>T
ENST00000485515.5:n.474+92C>T
ENST00000491274.5:c.498+92C>T ENSP00000480482.1:n.498+92C>T
NM_003000.2:c.540+92C>T , LRG_316t1:c.540+92C>T NP_002991.2:n.540+92C>T
NM_003000.3:c.540+92C>T MANE Select NP_002991.2:n.540+92C>T