Canonical Allele Identifier: CA2643677523
Gene: SDHB HGNC NCBI

Linked Data

gnomAD v4: 1-17027666-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17027666T>C , CM000663.2:g.17027666T>C GRCh38
NC_000001.10:g.17354161T>C , CM000663.1:g.17354161T>C GRCh37
NC_000001.9:g.17226748T>C NCBI36
NG_012340.1:g.31505A>G , LRG_316:g.31505A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.369+83A>G ENSP00000481376.2:n.369+83A>G
ENST00000491274.6:c.498+83A>G ENSP00000480482.2:n.498+83A>G
ENST00000375499.8:c.540+83A>G MANE Select ENSP00000364649.3:n.540+83A>G
ENST00000375499.7:c.540+83A>G ENSP00000364649.3:n.540+83A>G
ENST00000475506.1:n.540A>G
ENST00000485515.5:n.474+83A>G
ENST00000491274.5:c.498+83A>G ENSP00000480482.1:n.498+83A>G
NM_003000.2:c.540+83A>G , LRG_316t1:c.540+83A>G NP_002991.2:n.540+83A>G
NM_003000.3:c.540+83A>G MANE Select NP_002991.2:n.540+83A>G