Canonical Allele Identifier: CA2643677472
Gene: SDHB HGNC NCBI

Linked Data

gnomAD v4: 1-17027619-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17027619C>A , CM000663.2:g.17027619C>A GRCh38
NC_000001.10:g.17354114C>A , CM000663.1:g.17354114C>A GRCh37
NC_000001.9:g.17226701C>A NCBI36
NG_012340.1:g.31552G>T , LRG_316:g.31552G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.369+130G>T ENSP00000481376.2:n.369+130G>T
ENST00000491274.6:c.498+130G>T ENSP00000480482.2:n.498+130G>T
ENST00000375499.8:c.540+130G>T MANE Select ENSP00000364649.3:n.540+130G>T
ENST00000375499.7:c.540+130G>T ENSP00000364649.3:n.540+130G>T
ENST00000485515.5:n.474+130G>T
ENST00000491274.5:c.498+130G>T ENSP00000480482.1:n.498+130G>T
NM_003000.2:c.540+130G>T , LRG_316t1:c.540+130G>T NP_002991.2:n.540+130G>T
NM_003000.3:c.540+130G>T MANE Select NP_002991.2:n.540+130G>T