Canonical Allele Identifier: CA338272779

Gene: SDHB

Linked Data

• ClinVar Variation Id: 1400077
• ClinVar RCV Id: RCV001918002
• dbSNP Id: rs2101521715
• MyVariant Identifiers: chr1:g.17354300C>A (hg19) ; chr1:g.17027805C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027805C>A , CM000663.2:g.17027805C>A	GRCh38
NC_000001.10:g.17354300C>A , CM000663.1:g.17354300C>A	GRCh37
NC_000001.9:g.17226887C>A	NCBI36
NG_012340.1:g.31366G>T , LRG_316:g.31366G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.313G>T	ENSP00000481376.2:p.Glu105Ter
ENST00000491274.6:c.442G>T	ENSP00000480482.2:p.Glu148Ter
ENST00000375499.8:c.484G>T MANE Select	ENSP00000364649.3:p.Glu162Ter
ENST00000375499.7:c.484G>T	ENSP00000364649.3:p.Glu162Ter
ENST00000463045.2:c.313G>T	ENSP00000481376.1:p.Glu105Ter
ENST00000475506.1:n.401G>T
ENST00000485515.5:n.418G>T
ENST00000491274.5:c.442G>T	ENSP00000480482.1:p.Glu148Ter
NM_003000.2:c.484G>T , LRG_316t1:c.484G>T	NP_002991.2:p.Glu162Ter
NM_003000.3:c.484G>T MANE Select	NP_002991.2:p.Glu162Ter