Canonical Allele Identifier: CA1156080098
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs2077998265
gnomAD v3: 1-17027615-C-T
gnomAD v4: 1-17027615-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17027615C>T , CM000663.2:g.17027615C>T GRCh38
NC_000001.10:g.17354110C>T , CM000663.1:g.17354110C>T GRCh37
NC_000001.9:g.17226697C>T NCBI36
NG_012340.1:g.31556G>A , LRG_316:g.31556G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.369+134G>A ENSP00000481376.2:n.369+134G>A
ENST00000491274.6:c.498+134G>A ENSP00000480482.2:n.498+134G>A
ENST00000375499.8:c.540+134G>A MANE Select ENSP00000364649.3:n.540+134G>A
ENST00000375499.7:c.540+134G>A ENSP00000364649.3:n.540+134G>A
ENST00000485515.5:n.474+134G>A
ENST00000491274.5:c.498+134G>A ENSP00000480482.1:n.498+134G>A
NM_003000.2:c.540+134G>A , LRG_316t1:c.540+134G>A NP_002991.2:n.540+134G>A
NM_003000.3:c.540+134G>A MANE Select NP_002991.2:n.540+134G>A
Search 100 bp 5'
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