Canonical Allele Identifier: CA18662020

Gene: SDHB

Linked Data

• dbSNP Id: rs34604620
• MyVariant Identifiers: chr1:g.17348966_17348967insA (hg19) ; chr1:g.17022471_17022472insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17022474dup , CM000663.2:g.17022474dup	GRCh38
NC_000001.10:g.17348969dup , CM000663.1:g.17348969dup	GRCh37
NC_000001.9:g.17221556dup	NCBI36
NG_012340.1:g.36699dup , LRG_316:g.36699dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.594+136dup	ENSP00000481376.2:n.594+136dup
ENST00000491274.6:c.723+136dup	ENSP00000480482.2:n.723+136dup
ENST00000375499.8:c.765+136dup MANE Select	ENSP00000364649.3:n.765+136dup
ENST00000375499.7:c.765+136dup	ENSP00000364649.3:n.765+136dup
ENST00000475049.5:n.190+136dup
ENST00000485092.5:n.429+136dup
NM_003000.2:c.765+136dup , LRG_316t1:c.765+136dup	NP_002991.2:n.765+136dup
NM_003000.3:c.765+136dup MANE Select	NP_002991.2:n.765+136dup