Canonical Allele Identifier: CA2499214288
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 1111318
ClinVar RCV Id: RCV001437867
dbSNP Id: rs1553177265
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022600C>A , CM000663.2:g.17022600C>A GRCh38
NC_000001.10:g.17349095C>A , CM000663.1:g.17349095C>A GRCh37
NC_000001.9:g.17221682C>A NCBI36
NG_012340.1:g.36571G>T , LRG_316:g.36571G>T

Transcript Alleles

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