Canonical Allele Identifier: CA2643678636

Gene: SDHB

Linked Data

• gnomAD v4: 1-17028505-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17028505C>A , CM000663.2:g.17028505C>A	GRCh38
NC_000001.10:g.17355000C>A , CM000663.1:g.17355000C>A	GRCh37
NC_000001.9:g.17227587C>A	NCBI36
NG_012340.1:g.30666G>T , LRG_316:g.30666G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.252+95G>T	ENSP00000481376.2:n.252+95G>T
ENST00000491274.6:c.381+95G>T	ENSP00000480482.2:n.381+95G>T
ENST00000375499.8:c.423+95G>T MANE Select	ENSP00000364649.3:n.423+95G>T
ENST00000375499.7:c.423+95G>T	ENSP00000364649.3:n.423+95G>T
ENST00000463045.2:c.252+95G>T	ENSP00000481376.1:n.252+95G>T
ENST00000475506.1:n.340+95G>T
ENST00000485515.5:n.357+149G>T
ENST00000491274.5:c.381+95G>T	ENSP00000480482.1:n.381+95G>T
NM_003000.2:c.423+95G>T , LRG_316t1:c.423+95G>T	NP_002991.2:n.423+95G>T
NM_003000.3:c.423+95G>T MANE Select	NP_002991.2:n.423+95G>T