Canonical Allele Identifier: CA890984684
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs1195163722
MyVariant Identifiers: chr1:g.17348677T>G (hg19) chr1:g.17022182T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022182T>G , CM000663.2:g.17022182T>G GRCh38
NC_000001.10:g.17348677T>G , CM000663.1:g.17348677T>G GRCh37
NC_000001.9:g.17221264T>G NCBI36
NG_012340.1:g.36989A>C , LRG_316:g.36989A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.594+426A>C ENSP00000481376.2:n.594+426A>C
ENST00000491274.6:c.723+426A>C ENSP00000480482.2:n.723+426A>C
ENST00000375499.8:c.765+426A>C MANE Select ENSP00000364649.3:n.765+426A>C
ENST00000375499.7:c.765+426A>C ENSP00000364649.3:n.765+426A>C
ENST00000475049.5:n.190+426A>C
ENST00000485092.5:n.429+426A>C
NM_003000.2:c.765+426A>C , LRG_316t1:c.765+426A>C NP_002991.2:n.765+426A>C
NM_003000.3:c.765+426A>C MANE Select NP_002991.2:n.765+426A>C
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