Canonical Allele Identifier: CA338270021
Gene: SDHB HGNC NCBI

Linked Data

gnomAD v4: 1-17022622-T-C
MyVariant Identifiers: chr1:g.17349117T>C (hg19) chr1:g.17022622T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022622T>C , CM000663.2:g.17022622T>C GRCh38
NC_000001.10:g.17349117T>C , CM000663.1:g.17349117T>C GRCh37
NC_000001.9:g.17221704T>C NCBI36
NG_012340.1:g.36549A>G , LRG_316:g.36549A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.580A>G ENSP00000481376.2:p.Arg194Gly
ENST00000491274.6:c.709A>G ENSP00000480482.2:p.Arg237Gly
ENST00000375499.8:c.751A>G MANE Select ENSP00000364649.3:p.Arg251Gly
ENST00000375499.7:c.751A>G ENSP00000364649.3:p.Arg251Gly
ENST00000475049.5:n.176A>G
ENST00000485092.5:n.415A>G
ENST00000485515.5:n.685A>G
NM_003000.2:c.751A>G , LRG_316t1:c.751A>G NP_002991.2:p.Arg251Gly
NM_003000.3:c.751A>G MANE Select NP_002991.2:p.Arg251Gly
Search 100 bp 5'
Search 100 bp 3'