Canonical Allele Identifier: CA338275120

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17355217A>T (hg19) ; chr1:g.17028722A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17028722A>T , CM000663.2:g.17028722A>T	GRCh38
NC_000001.10:g.17355217A>T , CM000663.1:g.17355217A>T	GRCh37
NC_000001.9:g.17227804A>T	NCBI36
NG_012340.1:g.30449T>A , LRG_316:g.30449T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.130T>A	ENSP00000481376.2:p.Cys44Ser
ENST00000491274.6:c.259T>A	ENSP00000480482.2:p.Cys87Ser
ENST00000375499.8:c.301T>A MANE Select	ENSP00000364649.3:p.Cys101Ser
ENST00000375499.7:c.301T>A	ENSP00000364649.3:p.Cys101Ser
ENST00000463045.2:c.130T>A	ENSP00000481376.1:p.Cys44Ser
ENST00000475506.1:n.218T>A
ENST00000485515.5:n.289T>A
ENST00000491274.5:c.259T>A	ENSP00000480482.1:p.Cys87Ser
NM_003000.2:c.301T>A , LRG_316t1:c.301T>A	NP_002991.2:p.Cys101Ser
NM_003000.3:c.301T>A MANE Select	NP_002991.2:p.Cys101Ser