Canonical Allele Identifier: CA416081617
Gene: SDHB HGNC NCBI

Linked Data

gnomAD v4: 1-17022507-A-G
MyVariant Identifiers: chr1:g.17349002A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022507A>G , CM000663.2:g.17022507A>G GRCh38
NC_000001.10:g.17349002A>G , CM000663.1:g.17349002A>G GRCh37
NC_000001.9:g.17221589A>G NCBI36
NG_012340.1:g.36664T>C , LRG_316:g.36664T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.594+101T>C ENSP00000481376.2:n.594+101T>C
ENST00000491274.6:c.723+101T>C ENSP00000480482.2:n.723+101T>C
ENST00000375499.8:c.765+101T>C MANE Select ENSP00000364649.3:n.765+101T>C
ENST00000375499.7:c.765+101T>C ENSP00000364649.3:n.765+101T>C
ENST00000475049.5:n.190+101T>C
ENST00000485092.5:n.429+101T>C
NM_003000.2:c.765+101T>C , LRG_316t1:c.765+101T>C NP_002991.2:n.765+101T>C
NM_003000.3:c.765+101T>C MANE Select NP_002991.2:n.765+101T>C
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