Canonical Allele Identifier: CA18663086
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs554067534
gnomAD v3: 1-17023906-A-G
gnomAD v4: 1-17023906-A-G
MyVariant Identifiers: chr1:g.17350401A>G (hg19) chr1:g.17023906A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17023906A>G , CM000663.2:g.17023906A>G GRCh38
NC_000001.10:g.17350401A>G , CM000663.1:g.17350401A>G GRCh37
NC_000001.9:g.17222988A>G NCBI36
NG_012340.1:g.35265T>C , LRG_316:g.35265T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.471+67T>C ENSP00000481376.2:n.471+67T>C
ENST00000491274.6:c.600+67T>C ENSP00000480482.2:n.600+67T>C
ENST00000375499.8:c.642+67T>C MANE Select ENSP00000364649.3:n.642+67T>C
ENST00000375499.7:c.642+67T>C ENSP00000364649.3:n.642+67T>C
ENST00000485515.5:n.576+67T>C
NM_003000.2:c.642+67T>C , LRG_316t1:c.642+67T>C NP_002991.2:n.642+67T>C
NM_003000.3:c.642+67T>C MANE Select NP_002991.2:n.642+67T>C
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