Canonical Allele Identifier: CA416086106

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17354313C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027818C>T , CM000663.2:g.17027818C>T	GRCh38
NC_000001.10:g.17354313C>T , CM000663.1:g.17354313C>T	GRCh37
NC_000001.9:g.17226900C>T	NCBI36
NG_012340.1:g.31353G>A , LRG_316:g.31353G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.300G>A	ENSP00000481376.2:p.Leu100=
ENST00000491274.6:c.429G>A	ENSP00000480482.2:p.Leu143=
ENST00000375499.8:c.471G>A MANE Select	ENSP00000364649.3:p.Leu157=
ENST00000375499.7:c.471G>A	ENSP00000364649.3:p.Leu157=
ENST00000463045.2:c.300G>A	ENSP00000481376.1:p.Leu100=
ENST00000475506.1:n.388G>A
ENST00000485515.5:n.405G>A
ENST00000491274.5:c.429G>A	ENSP00000480482.1:p.Leu143=
NM_003000.2:c.471G>A , LRG_316t1:c.471G>A	NP_002991.2:p.Leu157=
NM_003000.3:c.471G>A MANE Select	NP_002991.2:p.Leu157=