Canonical Allele Identifier: CA089579
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 2925192
ClinVar RCV Id: RCV003780846
dbSNP Id: rs775784091
ExAC: 1:17355240 G / T
gnomAD v2: 1-17355240-G-T
gnomAD v3: 1-17028745-G-T
gnomAD v4: 1-17028745-G-T
MyVariant Identifiers: chr1:g.17355240G>T (hg19) chr1:g.17028745G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17028745G>T , CM000663.2:g.17028745G>T GRCh38
NC_000001.10:g.17355240G>T , CM000663.1:g.17355240G>T GRCh37
NC_000001.9:g.17227827G>T NCBI36
NG_012340.1:g.30426C>A , LRG_316:g.30426C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.116-9C>A ENSP00000481376.2:n.116-9C>A
ENST00000491274.6:c.245-9C>A ENSP00000480482.2:n.245-9C>A
ENST00000375499.8:c.287-9C>A MANE Select ENSP00000364649.3:n.287-9C>A
ENST00000375499.7:c.287-9C>A ENSP00000364649.3:n.287-9C>A
ENST00000463045.2:c.116-9C>A ENSP00000481376.1:n.116-9C>A
ENST00000475506.1:n.204-9C>A
ENST00000485515.5:n.275-9C>A
ENST00000491274.5:c.245-9C>A ENSP00000480482.1:n.245-9C>A
NM_003000.2:c.287-9C>A , LRG_316t1:c.287-9C>A NP_002991.2:n.287-9C>A
NM_003000.3:c.287-9C>A MANE Select NP_002991.2:n.287-9C>A
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