Canonical Allele Identifier: CA338272767

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17354298T>G (hg19) ; chr1:g.17027803T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027803T>G , CM000663.2:g.17027803T>G	GRCh38
NC_000001.10:g.17354298T>G , CM000663.1:g.17354298T>G	GRCh37
NC_000001.9:g.17226885T>G	NCBI36
NG_012340.1:g.31368A>C , LRG_316:g.31368A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.315A>C	ENSP00000481376.2:p.Glu105Asp
ENST00000491274.6:c.444A>C	ENSP00000480482.2:p.Glu148Asp
ENST00000375499.8:c.486A>C MANE Select	ENSP00000364649.3:p.Glu162Asp
ENST00000375499.7:c.486A>C	ENSP00000364649.3:p.Glu162Asp
ENST00000463045.2:c.315A>C	ENSP00000481376.1:p.Glu105Asp
ENST00000475506.1:n.403A>C
ENST00000485515.5:n.420A>C
ENST00000491274.5:c.444A>C	ENSP00000480482.1:p.Glu148Asp
NM_003000.2:c.486A>C , LRG_316t1:c.486A>C	NP_002991.2:p.Glu162Asp
NM_003000.3:c.486A>C MANE Select	NP_002991.2:p.Glu162Asp