Canonical Allele Identifier: CA338228422
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs1570958165
gnomAD v4: 1-17044885-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17044885A>G , CM000663.2:g.17044885A>G GRCh38
NC_000001.10:g.17371380A>G , CM000663.1:g.17371380A>G GRCh37
NC_000001.9:g.17243967A>G NCBI36
NG_012340.1:g.14286T>C , LRG_316:g.14286T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.-96T>C ENSP00000481376.2:n.-96T>C
ENST00000491274.6:c.34T>C ENSP00000480482.2:p.Ser12Pro
ENST00000375499.8:c.76T>C MANE Select ENSP00000364649.3:p.Ser26Pro
ENST00000375499.7:c.76T>C ENSP00000364649.3:p.Ser26Pro
ENST00000463045.2:c.-96T>C ENSP00000481376.1:n.-96T>C
ENST00000466613.2:n.88T>C
ENST00000485515.5:n.64T>C
ENST00000491274.5:c.34T>C ENSP00000480482.1:p.Ser12Pro
NM_003000.2:c.76T>C , LRG_316t1:c.76T>C NP_002991.2:p.Ser26Pro
NM_003000.3:c.76T>C MANE Select NP_002991.2:p.Ser26Pro