Canonical Allele Identifier: CA890972343

Gene: SDHB

Linked Data

• dbSNP Id: rs1439747464
• MyVariant Identifiers: chr1:g.17355004C>T (hg19) ; chr1:g.17028509C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17028509C>T , CM000663.2:g.17028509C>T	GRCh38
NC_000001.10:g.17355004C>T , CM000663.1:g.17355004C>T	GRCh37
NC_000001.9:g.17227591C>T	NCBI36
NG_012340.1:g.30662G>A , LRG_316:g.30662G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.252+91G>A	ENSP00000481376.2:n.252+91G>A
ENST00000491274.6:c.381+91G>A	ENSP00000480482.2:n.381+91G>A
ENST00000375499.8:c.423+91G>A MANE Select	ENSP00000364649.3:n.423+91G>A
ENST00000375499.7:c.423+91G>A	ENSP00000364649.3:n.423+91G>A
ENST00000463045.2:c.252+91G>A	ENSP00000481376.1:n.252+91G>A
ENST00000475506.1:n.340+91G>A
ENST00000485515.5:n.357+145G>A
ENST00000491274.5:c.381+91G>A	ENSP00000480482.1:n.381+91G>A
NM_003000.2:c.423+91G>A , LRG_316t1:c.423+91G>A	NP_002991.2:n.423+91G>A
NM_003000.3:c.423+91G>A MANE Select	NP_002991.2:n.423+91G>A