Canonical Allele Identifier: CA645671421
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs1337755155
gnomAD v3: 1-17022510-G-C
gnomAD v4: 1-17022510-G-C
COSMIC: COSN1413613 COSN5357825
MyVariant Identifiers: chr1:g.17349005G>C (hg19) chr1:g.17022510G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022510G>C , CM000663.2:g.17022510G>C GRCh38
NC_000001.10:g.17349005G>C , CM000663.1:g.17349005G>C GRCh37
NC_000001.9:g.17221592G>C NCBI36
NG_012340.1:g.36661C>G , LRG_316:g.36661C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.594+98C>G ENSP00000481376.2:n.594+98C>G
ENST00000491274.6:c.723+98C>G ENSP00000480482.2:n.723+98C>G
ENST00000375499.8:c.765+98C>G MANE Select ENSP00000364649.3:n.765+98C>G
ENST00000375499.7:c.765+98C>G ENSP00000364649.3:n.765+98C>G
ENST00000475049.5:n.190+98C>G
ENST00000485092.5:n.429+98C>G
NM_003000.2:c.765+98C>G , LRG_316t1:c.765+98C>G NP_002991.2:n.765+98C>G
NM_003000.3:c.765+98C>G MANE Select NP_002991.2:n.765+98C>G
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