Canonical Allele Identifier: CA416087613

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17355131A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17028636A>G , CM000663.2:g.17028636A>G	GRCh38
NC_000001.10:g.17355131A>G , CM000663.1:g.17355131A>G	GRCh37
NC_000001.9:g.17227718A>G	NCBI36
NG_012340.1:g.30535T>C , LRG_316:g.30535T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.216T>C	ENSP00000481376.2:p.Pro72=
ENST00000491274.6:c.345T>C	ENSP00000480482.2:p.Pro115=
ENST00000375499.8:c.387T>C MANE Select	ENSP00000364649.3:p.Pro129=
ENST00000375499.7:c.387T>C	ENSP00000364649.3:p.Pro129=
ENST00000463045.2:c.216T>C	ENSP00000481376.1:p.Pro72=
ENST00000475506.1:n.304T>C
ENST00000485515.5:n.357+18T>C
ENST00000491274.5:c.345T>C	ENSP00000480482.1:p.Pro115=
NM_003000.2:c.387T>C , LRG_316t1:c.387T>C	NP_002991.2:p.Pro129=
NM_003000.3:c.387T>C MANE Select	NP_002991.2:p.Pro129=