Canonical Allele Identifier: CA416047115

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17371354G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17044859G>T , CM000663.2:g.17044859G>T	GRCh38
NC_000001.10:g.17371354G>T , CM000663.1:g.17371354G>T	GRCh37
NC_000001.9:g.17243941G>T	NCBI36
NG_012340.1:g.14312C>A , LRG_316:g.14312C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.-70C>A	ENSP00000481376.2:n.-70C>A
ENST00000491274.6:c.60C>A	ENSP00000480482.2:p.Ala20=
ENST00000375499.8:c.102C>A MANE Select	ENSP00000364649.3:p.Ala34=
ENST00000375499.7:c.102C>A	ENSP00000364649.3:p.Ala34=
ENST00000463045.2:c.-70C>A	ENSP00000481376.1:n.-70C>A
ENST00000466613.2:n.114C>A
ENST00000475506.1:n.19C>A
ENST00000485515.5:n.90C>A
ENST00000491274.5:c.60C>A	ENSP00000480482.1:p.Ala20=
NM_003000.2:c.102C>A , LRG_316t1:c.102C>A	NP_002991.2:p.Ala34=
NM_003000.3:c.102C>A MANE Select	NP_002991.2:p.Ala34=