Canonical Allele Identifier: CA416089451

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17359613T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17033118T>C , CM000663.2:g.17033118T>C	GRCh38
NC_000001.10:g.17359613T>C , CM000663.1:g.17359613T>C	GRCh37
NC_000001.9:g.17232200T>C	NCBI36
NG_012340.1:g.26053A>G , LRG_316:g.26053A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.57A>G	ENSP00000481376.2:p.Leu19=
ENST00000491274.6:c.186A>G	ENSP00000480482.2:p.Leu62=
ENST00000375499.8:c.228A>G MANE Select	ENSP00000364649.3:p.Leu76=
ENST00000375499.7:c.228A>G	ENSP00000364649.3:p.Leu76=
ENST00000463045.2:c.57A>G	ENSP00000481376.1:p.Leu19=
ENST00000466613.2:n.240A>G
ENST00000475506.1:n.145A>G
ENST00000485515.5:n.216A>G
ENST00000491274.5:c.186A>G	ENSP00000480482.1:p.Leu62=
NM_003000.2:c.228A>G , LRG_316t1:c.228A>G	NP_002991.2:p.Leu76=
NM_003000.3:c.228A>G MANE Select	NP_002991.2:p.Leu76=