Canonical Allele Identifier: CA338270463
Gene: SDHB HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.17349205G>C (hg19) chr1:g.17022710G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022710G>C , CM000663.2:g.17022710G>C GRCh38
NC_000001.10:g.17349205G>C , CM000663.1:g.17349205G>C GRCh37
NC_000001.9:g.17221792G>C NCBI36
NG_012340.1:g.36461C>G , LRG_316:g.36461C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.492C>G ENSP00000481376.2:p.Asp164Glu
ENST00000491274.6:c.621C>G ENSP00000480482.2:p.Asp207Glu
ENST00000375499.8:c.663C>G MANE Select ENSP00000364649.3:p.Asp221Glu
ENST00000375499.7:c.663C>G ENSP00000364649.3:p.Asp221Glu
ENST00000475049.5:n.88C>G
ENST00000485092.5:n.327C>G
ENST00000485515.5:n.597C>G
NM_003000.2:c.663C>G , LRG_316t1:c.663C>G NP_002991.2:p.Asp221Glu
NM_003000.3:c.663C>G MANE Select NP_002991.2:p.Asp221Glu
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