Canonical Allele Identifier: CA2574235371
Gene: SDHB HGNC NCBI

Linked Data

gnomAD v4: 1-17023895-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17023895T>C , CM000663.2:g.17023895T>C GRCh38
NC_000001.10:g.17350390T>C , CM000663.1:g.17350390T>C GRCh37
NC_000001.9:g.17222977T>C NCBI36
NG_012340.1:g.35276A>G , LRG_316:g.35276A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.471+78A>G ENSP00000481376.2:n.471+78A>G
ENST00000491274.6:c.600+78A>G ENSP00000480482.2:n.600+78A>G
ENST00000375499.8:c.642+78A>G MANE Select ENSP00000364649.3:n.642+78A>G
ENST00000375499.7:c.642+78A>G ENSP00000364649.3:n.642+78A>G
ENST00000485515.5:n.576+78A>G
NM_003000.2:c.642+78A>G , LRG_316t1:c.642+78A>G NP_002991.2:n.642+78A>G
NM_003000.3:c.642+78A>G MANE Select NP_002991.2:n.642+78A>G