Canonical Allele Identifier: CA416088071

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17355212T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17028717T>A , CM000663.2:g.17028717T>A	GRCh38
NC_000001.10:g.17355212T>A , CM000663.1:g.17355212T>A	GRCh37
NC_000001.9:g.17227799T>A	NCBI36
NG_012340.1:g.30454A>T , LRG_316:g.30454A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.135A>T	ENSP00000481376.2:p.Ala45=
ENST00000491274.6:c.264A>T	ENSP00000480482.2:p.Ala88=
ENST00000375499.8:c.306A>T MANE Select	ENSP00000364649.3:p.Ala102=
ENST00000375499.7:c.306A>T	ENSP00000364649.3:p.Ala102=
ENST00000463045.2:c.135A>T	ENSP00000481376.1:p.Ala45=
ENST00000475506.1:n.223A>T
ENST00000485515.5:n.294A>T
ENST00000491274.5:c.264A>T	ENSP00000480482.1:p.Ala88=
NM_003000.2:c.306A>T , LRG_316t1:c.306A>T	NP_002991.2:p.Ala102=
NM_003000.3:c.306A>T MANE Select	NP_002991.2:p.Ala102=