Canonical Allele Identifier: CA338276418

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17359564A>T (hg19) ; chr1:g.17033069A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17033069A>T , CM000663.2:g.17033069A>T	GRCh38
NC_000001.10:g.17359564A>T , CM000663.1:g.17359564A>T	GRCh37
NC_000001.9:g.17232151A>T	NCBI36
NG_012340.1:g.26102T>A , LRG_316:g.26102T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.106T>A	ENSP00000481376.2:p.Cys36Ser
ENST00000491274.6:c.235T>A	ENSP00000480482.2:p.Cys79Ser
ENST00000375499.8:c.277T>A MANE Select	ENSP00000364649.3:p.Cys93Ser
ENST00000375499.7:c.277T>A	ENSP00000364649.3:p.Cys93Ser
ENST00000463045.2:c.106T>A	ENSP00000481376.1:p.Cys36Ser
ENST00000466613.2:n.289T>A
ENST00000475506.1:n.194T>A
ENST00000485515.5:n.265T>A
ENST00000491274.5:c.235T>A	ENSP00000480482.1:p.Cys79Ser
NM_003000.2:c.277T>A , LRG_316t1:c.277T>A	NP_002991.2:p.Cys93Ser
NM_003000.3:c.277T>A MANE Select	NP_002991.2:p.Cys93Ser