Canonical Allele Identifier: CA999081983
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs2077970764
gnomAD v3: 1-17023004-C-A
gnomAD v4: 1-17023004-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17023004C>A , CM000663.2:g.17023004C>A GRCh38
NC_000001.10:g.17349499C>A , CM000663.1:g.17349499C>A GRCh37
NC_000001.9:g.17222086C>A NCBI36
NG_012340.1:g.36167G>T , LRG_316:g.36167G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.472-274G>T ENSP00000481376.2:n.472-274G>T
ENST00000491274.6:c.601-274G>T ENSP00000480482.2:n.601-274G>T
ENST00000375499.8:c.643-274G>T MANE Select ENSP00000364649.3:n.643-274G>T
ENST00000375499.7:c.643-274G>T ENSP00000364649.3:n.643-274G>T
ENST00000475049.5:n.67+90G>T
ENST00000485092.5:n.33G>T
ENST00000485515.5:n.577-274G>T
NM_003000.2:c.643-274G>T , LRG_316t1:c.643-274G>T NP_002991.2:n.643-274G>T
NM_003000.3:c.643-274G>T MANE Select NP_002991.2:n.643-274G>T