Canonical Allele Identifier: CA2574235829
Gene: SDHB HGNC NCBI

Linked Data

gnomAD v4: 1-17027905-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17027905G>T , CM000663.2:g.17027905G>T GRCh38
NC_000001.10:g.17354400G>T , CM000663.1:g.17354400G>T GRCh37
NC_000001.9:g.17226987G>T NCBI36
NG_012340.1:g.31266C>A , LRG_316:g.31266C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.253-40C>A ENSP00000481376.2:n.253-40C>A
ENST00000491274.6:c.382-40C>A ENSP00000480482.2:n.382-40C>A
ENST00000375499.8:c.424-40C>A MANE Select ENSP00000364649.3:n.424-40C>A
ENST00000375499.7:c.424-40C>A ENSP00000364649.3:n.424-40C>A
ENST00000463045.2:c.253-40C>A ENSP00000481376.1:n.253-40C>A
ENST00000475506.1:n.341-40C>A
ENST00000485515.5:n.358-40C>A
ENST00000491274.5:c.382-40C>A ENSP00000480482.1:n.382-40C>A
NM_003000.2:c.424-40C>A , LRG_316t1:c.424-40C>A NP_002991.2:n.424-40C>A
NM_003000.3:c.424-40C>A MANE Select NP_002991.2:n.424-40C>A