Canonical Allele Identifier: CA416086012

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17354301A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027806A>G , CM000663.2:g.17027806A>G	GRCh38
NC_000001.10:g.17354301A>G , CM000663.1:g.17354301A>G	GRCh37
NC_000001.9:g.17226888A>G	NCBI36
NG_012340.1:g.31365T>C , LRG_316:g.31365T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.312T>C	ENSP00000481376.2:p.Asp104=
ENST00000491274.6:c.441T>C	ENSP00000480482.2:p.Asp147=
ENST00000375499.8:c.483T>C MANE Select	ENSP00000364649.3:p.Asp161=
ENST00000375499.7:c.483T>C	ENSP00000364649.3:p.Asp161=
ENST00000463045.2:c.312T>C	ENSP00000481376.1:p.Asp104=
ENST00000475506.1:n.400T>C
ENST00000485515.5:n.417T>C
ENST00000491274.5:c.441T>C	ENSP00000480482.1:p.Asp147=
NM_003000.2:c.483T>C , LRG_316t1:c.483T>C	NP_002991.2:p.Asp161=
NM_003000.3:c.483T>C MANE Select	NP_002991.2:p.Asp161=