Canonical Allele Identifier: CA2580060647

Gene: SDHB

Linked Data

• ClinVar Variation Id: 2097412
• ClinVar RCV Id: RCV003016687

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027746G>A , CM000663.2:g.17027746G>A	GRCh38
NC_000001.10:g.17354241G>A , CM000663.1:g.17354241G>A	GRCh37
NC_000001.9:g.17226828G>A	NCBI36
NG_012340.1:g.31425C>T , LRG_316:g.31425C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.369+3C>T	ENSP00000481376.2:n.369+3C>T
ENST00000491274.6:c.498+3C>T	ENSP00000480482.2:n.498+3C>T
ENST00000375499.8:c.540+3C>T MANE Select	ENSP00000364649.3:n.540+3C>T
ENST00000375499.7:c.540+3C>T	ENSP00000364649.3:n.540+3C>T
ENST00000475506.1:n.460C>T
ENST00000485515.5:n.474+3C>T
ENST00000491274.5:c.498+3C>T	ENSP00000480482.1:n.498+3C>T
NM_003000.2:c.540+3C>T , LRG_316t1:c.540+3C>T	NP_002991.2:n.540+3C>T
NM_003000.3:c.540+3C>T MANE Select	NP_002991.2:n.540+3C>T