Canonical Allele Identifier: CA521037606

Gene: SDHB

Linked Data

• dbSNP Id: rs1292128028
• gnomAD v2: 1-17349088-ACCAG-A
• gnomAD v4: 1-17022593-ACCAG-A
• MyVariant Identifiers: chr1:g.17349089_17349092del (hg19) ; chr1:g.17022594_17022597del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17022596_17022599del , CM000663.2:g.17022596_17022599del	GRCh38
NC_000001.10:g.17349091_17349094del , CM000663.1:g.17349091_17349094del	GRCh37
NC_000001.9:g.17221678_17221681del	NCBI36
NG_012340.1:g.36574_36577del , LRG_316:g.36574_36577del

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.594+11_594+14del	ENSP00000481376.2:n.594+11_594+14del
ENST00000491274.6:c.723+11_723+14del	ENSP00000480482.2:n.723+11_723+14del
ENST00000375499.8:c.765+11_765+14del MANE Select	ENSP00000364649.3:n.765+11_765+14del
ENST00000375499.7:c.765+11_765+14del	ENSP00000364649.3:n.765+11_765+14del
ENST00000475049.5:n.190+11_190+14del
ENST00000485092.5:n.429+11_429+14del
NM_003000.2:c.765+11_765+14del , LRG_316t1:c.765+11_765+14del	NP_002991.2:n.765+11_765+14del
NM_003000.3:c.765+11_765+14del MANE Select	NP_002991.2:n.765+11_765+14del