Canonical Allele Identifier: CA416088103

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17355218A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17028723A>C , CM000663.2:g.17028723A>C	GRCh38
NC_000001.10:g.17355218A>C , CM000663.1:g.17355218A>C	GRCh37
NC_000001.9:g.17227805A>C	NCBI36
NG_012340.1:g.30448T>G , LRG_316:g.30448T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.129T>G	ENSP00000481376.2:p.Ser43=
ENST00000491274.6:c.258T>G	ENSP00000480482.2:p.Ser86=
ENST00000375499.8:c.300T>G MANE Select	ENSP00000364649.3:p.Ser100=
ENST00000375499.7:c.300T>G	ENSP00000364649.3:p.Ser100=
ENST00000463045.2:c.129T>G	ENSP00000481376.1:p.Ser43=
ENST00000475506.1:n.217T>G
ENST00000485515.5:n.288T>G
ENST00000491274.5:c.258T>G	ENSP00000480482.1:p.Ser86=
NM_003000.2:c.300T>G , LRG_316t1:c.300T>G	NP_002991.2:p.Ser100=
NM_003000.3:c.300T>G MANE Select	NP_002991.2:p.Ser100=