Canonical Allele Identifier: CA521037582
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs1352422559
gnomAD v2: 1-17348975-G-C
gnomAD v3: 1-17022480-G-C
gnomAD v4: 1-17022480-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022480G>C , CM000663.2:g.17022480G>C GRCh38
NC_000001.10:g.17348975G>C , CM000663.1:g.17348975G>C GRCh37
NC_000001.9:g.17221562G>C NCBI36
NG_012340.1:g.36691C>G , LRG_316:g.36691C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.594+128C>G ENSP00000481376.2:n.594+128C>G
ENST00000491274.6:c.723+128C>G ENSP00000480482.2:n.723+128C>G
ENST00000375499.8:c.765+128C>G MANE Select ENSP00000364649.3:n.765+128C>G
ENST00000375499.7:c.765+128C>G ENSP00000364649.3:n.765+128C>G
ENST00000475049.5:n.190+128C>G
ENST00000485092.5:n.429+128C>G
NM_003000.2:c.765+128C>G , LRG_316t1:c.765+128C>G NP_002991.2:n.765+128C>G
NM_003000.3:c.765+128C>G MANE Select NP_002991.2:n.765+128C>G