Canonical Allele Identifier: CA416086202

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17354328G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027833G>C , CM000663.2:g.17027833G>C	GRCh38
NC_000001.10:g.17354328G>C , CM000663.1:g.17354328G>C	GRCh37
NC_000001.9:g.17226915G>C	NCBI36
NG_012340.1:g.31338C>G , LRG_316:g.31338C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.285C>G	ENSP00000481376.2:p.Ser95=
ENST00000491274.6:c.414C>G	ENSP00000480482.2:p.Ser138=
ENST00000375499.8:c.456C>G MANE Select	ENSP00000364649.3:p.Ser152=
ENST00000375499.7:c.456C>G	ENSP00000364649.3:p.Ser152=
ENST00000463045.2:c.285C>G	ENSP00000481376.1:p.Ser95=
ENST00000475506.1:n.373C>G
ENST00000485515.5:n.390C>G
ENST00000491274.5:c.414C>G	ENSP00000480482.1:p.Ser138=
NM_003000.2:c.456C>G , LRG_316t1:c.456C>G	NP_002991.2:p.Ser152=
NM_003000.3:c.456C>G MANE Select	NP_002991.2:p.Ser152=