Canonical Allele Identifier: CA338272500

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17354257T>G (hg19) ; chr1:g.17027762T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027762T>G , CM000663.2:g.17027762T>G	GRCh38
NC_000001.10:g.17354257T>G , CM000663.1:g.17354257T>G	GRCh37
NC_000001.9:g.17226844T>G	NCBI36
NG_012340.1:g.31409A>C , LRG_316:g.31409A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.356A>C	ENSP00000481376.2:p.Glu119Ala
ENST00000491274.6:c.485A>C	ENSP00000480482.2:p.Glu162Ala
ENST00000375499.8:c.527A>C MANE Select	ENSP00000364649.3:p.Glu176Ala
ENST00000375499.7:c.527A>C	ENSP00000364649.3:p.Glu176Ala
ENST00000463045.2:c.356A>C	ENSP00000481376.1:p.Glu119Ala
ENST00000475506.1:n.444A>C
ENST00000485515.5:n.461A>C
ENST00000491274.5:c.485A>C	ENSP00000480482.1:p.Glu162Ala
NM_003000.2:c.527A>C , LRG_316t1:c.527A>C	NP_002991.2:p.Glu176Ala
NM_003000.3:c.527A>C MANE Select	NP_002991.2:p.Glu176Ala