Canonical Allele Identifier: CA890984746

Gene: SDHB

Linked Data

• dbSNP Id: rs1275970559
• gnomAD v3: 1-17022304-TTC-T
• gnomAD v4: 1-17022304-TTC-T
• MyVariant Identifiers: chr1:g.17348800_17348801del (hg19) ; chr1:g.17022305_17022306del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17022306_17022307del , CM000663.2:g.17022306_17022307del	GRCh38
NC_000001.10:g.17348801_17348802del , CM000663.1:g.17348801_17348802del	GRCh37
NC_000001.9:g.17221388_17221389del	NCBI36
NG_012340.1:g.36865_36866del , LRG_316:g.36865_36866del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.594+302_594+303del	ENSP00000481376.2:n.594+302_594+303del
ENST00000491274.6:c.723+302_723+303del	ENSP00000480482.2:n.723+302_723+303del
ENST00000375499.8:c.765+302_765+303del MANE Select	ENSP00000364649.3:n.765+302_765+303del
ENST00000375499.7:c.765+302_765+303del	ENSP00000364649.3:n.765+302_765+303del
ENST00000475049.5:n.190+302_190+303del
ENST00000485092.5:n.429+302_429+303del
NM_003000.2:c.765+302_765+303del , LRG_316t1:c.765+302_765+303del	NP_002991.2:n.765+302_765+303del
NM_003000.3:c.765+302_765+303del MANE Select	NP_002991.2:n.765+302_765+303del