Canonical Allele Identifier: CA416081921
Gene: SDHB HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.17349151A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022656A>C , CM000663.2:g.17022656A>C GRCh38
NC_000001.10:g.17349151A>C , CM000663.1:g.17349151A>C GRCh37
NC_000001.9:g.17221738A>C NCBI36
NG_012340.1:g.36515T>G , LRG_316:g.36515T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.546T>G ENSP00000481376.2:p.Ser182=
ENST00000491274.6:c.675T>G ENSP00000480482.2:p.Ser225=
ENST00000375499.8:c.717T>G MANE Select ENSP00000364649.3:p.Ser239=
ENST00000375499.7:c.717T>G ENSP00000364649.3:p.Ser239=
ENST00000475049.5:n.142T>G
ENST00000485092.5:n.381T>G
ENST00000485515.5:n.651T>G
NM_003000.2:c.717T>G , LRG_316t1:c.717T>G NP_002991.2:p.Ser239=
NM_003000.3:c.717T>G MANE Select NP_002991.2:p.Ser239=
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