Canonical Allele Identifier: CA18661729
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs376027699
gnomAD v3: 1-17022127-A-G
gnomAD v4: 1-17022127-A-G
MyVariant Identifiers: chr1:g.17348622A>G (hg19) chr1:g.17022127A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022127A>G , CM000663.2:g.17022127A>G GRCh38
NC_000001.10:g.17348622A>G , CM000663.1:g.17348622A>G GRCh37
NC_000001.9:g.17221209A>G NCBI36
NG_012340.1:g.37044T>C , LRG_316:g.37044T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.594+481T>C ENSP00000481376.2:n.594+481T>C
ENST00000491274.6:c.723+481T>C ENSP00000480482.2:n.723+481T>C
ENST00000375499.8:c.765+481T>C MANE Select ENSP00000364649.3:n.765+481T>C
ENST00000375499.7:c.765+481T>C ENSP00000364649.3:n.765+481T>C
ENST00000475049.5:n.190+481T>C
ENST00000485092.5:n.429+481T>C
NM_003000.2:c.765+481T>C , LRG_316t1:c.765+481T>C NP_002991.2:n.765+481T>C
NM_003000.3:c.765+481T>C MANE Select NP_002991.2:n.765+481T>C
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