Canonical Allele Identifier: CA338274233

Gene: SDHB

Linked Data

• COSMIC: COSM5927183
• MyVariant Identifiers: chr1:g.17355127G>A (hg19) ; chr1:g.17028632G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17028632G>A , CM000663.2:g.17028632G>A	GRCh38
NC_000001.10:g.17355127G>A , CM000663.1:g.17355127G>A	GRCh37
NC_000001.9:g.17227714G>A	NCBI36
NG_012340.1:g.30539C>T , LRG_316:g.30539C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.220C>T	ENSP00000481376.2:p.Pro74Ser
ENST00000491274.6:c.349C>T	ENSP00000480482.2:p.Pro117Ser
ENST00000375499.8:c.391C>T MANE Select	ENSP00000364649.3:p.Pro131Ser
ENST00000375499.7:c.391C>T	ENSP00000364649.3:p.Pro131Ser
ENST00000463045.2:c.220C>T	ENSP00000481376.1:p.Pro74Ser
ENST00000475506.1:n.308C>T
ENST00000485515.5:n.357+22C>T
ENST00000491274.5:c.349C>T	ENSP00000480482.1:p.Pro117Ser
NM_003000.2:c.391C>T , LRG_316t1:c.391C>T	NP_002991.2:p.Pro131Ser
NM_003000.3:c.391C>T MANE Select	NP_002991.2:p.Pro131Ser