Canonical Allele Identifier: CA890985783

Gene: SDHB

Linked Data

• dbSNP Id: rs1205970531
• gnomAD v4: 1-17023894-T-A
• MyVariant Identifiers: chr1:g.17350389T>A (hg19) ; chr1:g.17023894T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17023894T>A , CM000663.2:g.17023894T>A	GRCh38
NC_000001.10:g.17350389T>A , CM000663.1:g.17350389T>A	GRCh37
NC_000001.9:g.17222976T>A	NCBI36
NG_012340.1:g.35277A>T , LRG_316:g.35277A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.471+79A>T	ENSP00000481376.2:n.471+79A>T
ENST00000491274.6:c.600+79A>T	ENSP00000480482.2:n.600+79A>T
ENST00000375499.8:c.642+79A>T MANE Select	ENSP00000364649.3:n.642+79A>T
ENST00000375499.7:c.642+79A>T	ENSP00000364649.3:n.642+79A>T
ENST00000485515.5:n.576+79A>T
NM_003000.2:c.642+79A>T , LRG_316t1:c.642+79A>T	NP_002991.2:n.642+79A>T
NM_003000.3:c.642+79A>T MANE Select	NP_002991.2:n.642+79A>T