Canonical Allele Identifier: CA089642
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 1652736
ClinVar RCV Id: RCV002173858
dbSNP Id: rs756714182
ExAC: 1:17354229 A / G
gnomAD v2: 1-17354229-A-G
gnomAD v4: 1-17027734-A-G
MyVariant Identifiers: chr1:g.17354229A>G (hg19) chr1:g.17027734A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17027734A>G , CM000663.2:g.17027734A>G GRCh38
NC_000001.10:g.17354229A>G , CM000663.1:g.17354229A>G GRCh37
NC_000001.9:g.17226816A>G NCBI36
NG_012340.1:g.31437T>C , LRG_316:g.31437T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.369+15T>C ENSP00000481376.2:n.369+15T>C
ENST00000491274.6:c.498+15T>C ENSP00000480482.2:n.498+15T>C
ENST00000375499.8:c.540+15T>C MANE Select ENSP00000364649.3:n.540+15T>C
ENST00000375499.7:c.540+15T>C ENSP00000364649.3:n.540+15T>C
ENST00000475506.1:n.472T>C
ENST00000485515.5:n.474+15T>C
ENST00000491274.5:c.498+15T>C ENSP00000480482.1:n.498+15T>C
NM_003000.2:c.540+15T>C , LRG_316t1:c.540+15T>C NP_002991.2:n.540+15T>C
NM_003000.3:c.540+15T>C MANE Select NP_002991.2:n.540+15T>C
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