Canonical Allele Identifier: CA1156078584
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs2077976897
gnomAD v4: 1-17023920-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17023920C>A , CM000663.2:g.17023920C>A GRCh38
NC_000001.10:g.17350415C>A , CM000663.1:g.17350415C>A GRCh37
NC_000001.9:g.17223002C>A NCBI36
NG_012340.1:g.35251G>T , LRG_316:g.35251G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.471+53G>T ENSP00000481376.2:n.471+53G>T
ENST00000491274.6:c.600+53G>T ENSP00000480482.2:n.600+53G>T
ENST00000375499.8:c.642+53G>T MANE Select ENSP00000364649.3:n.642+53G>T
ENST00000375499.7:c.642+53G>T ENSP00000364649.3:n.642+53G>T
ENST00000485515.5:n.576+53G>T
NM_003000.2:c.642+53G>T , LRG_316t1:c.642+53G>T NP_002991.2:n.642+53G>T
NM_003000.3:c.642+53G>T MANE Select NP_002991.2:n.642+53G>T
Search 100 bp 5'
Search 100 bp 3'