Canonical Allele Identifier: CA416085874
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs2101521640
MyVariant Identifiers: chr1:g.17354280C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17027785C>T , CM000663.2:g.17027785C>T GRCh38
NC_000001.10:g.17354280C>T , CM000663.1:g.17354280C>T GRCh37
NC_000001.9:g.17226867C>T NCBI36
NG_012340.1:g.31386G>A , LRG_316:g.31386G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.333G>A ENSP00000481376.2:p.Gln111=
ENST00000491274.6:c.462G>A ENSP00000480482.2:p.Gln154=
ENST00000375499.8:c.504G>A MANE Select ENSP00000364649.3:p.Gln168=
ENST00000375499.7:c.504G>A ENSP00000364649.3:p.Gln168=
ENST00000463045.2:c.333G>A ENSP00000481376.1:p.Gln111=
ENST00000475506.1:n.421G>A
ENST00000485515.5:n.438G>A
ENST00000491274.5:c.462G>A ENSP00000480482.1:p.Gln154=
NM_003000.2:c.504G>A , LRG_316t1:c.504G>A NP_002991.2:p.Gln168=
NM_003000.3:c.504G>A MANE Select NP_002991.2:p.Gln168=