Canonical Allele Identifier: CA2643678591

Gene: SDHB

Linked Data

• gnomAD v4: 1-17028471-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17028471T>G , CM000663.2:g.17028471T>G	GRCh38
NC_000001.10:g.17354966T>G , CM000663.1:g.17354966T>G	GRCh37
NC_000001.9:g.17227553T>G	NCBI36
NG_012340.1:g.30700A>C , LRG_316:g.30700A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.252+129A>C	ENSP00000481376.2:n.252+129A>C
ENST00000491274.6:c.381+129A>C	ENSP00000480482.2:n.381+129A>C
ENST00000375499.8:c.423+129A>C MANE Select	ENSP00000364649.3:n.423+129A>C
ENST00000375499.7:c.423+129A>C	ENSP00000364649.3:n.423+129A>C
ENST00000463045.2:c.252+129A>C	ENSP00000481376.1:n.252+129A>C
ENST00000475506.1:n.340+129A>C
ENST00000485515.5:n.357+183A>C
ENST00000491274.5:c.381+129A>C	ENSP00000480482.1:n.381+129A>C
NM_003000.2:c.423+129A>C , LRG_316t1:c.423+129A>C	NP_002991.2:n.423+129A>C
NM_003000.3:c.423+129A>C MANE Select	NP_002991.2:n.423+129A>C