Canonical Allele Identifier: CA2643678296

Gene: SDHB

Linked Data

• gnomAD v4: 1-17028853-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17028853T>G , CM000663.2:g.17028853T>G	GRCh38
NC_000001.10:g.17355348T>G , CM000663.1:g.17355348T>G	GRCh37
NC_000001.9:g.17227935T>G	NCBI36
NG_012340.1:g.30318A>C , LRG_316:g.30318A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.116-117A>C	ENSP00000481376.2:n.116-117A>C
ENST00000491274.6:c.245-117A>C	ENSP00000480482.2:n.245-117A>C
ENST00000375499.8:c.287-117A>C MANE Select	ENSP00000364649.3:n.287-117A>C
ENST00000375499.7:c.287-117A>C	ENSP00000364649.3:n.287-117A>C
ENST00000463045.2:c.116-117A>C	ENSP00000481376.1:n.116-117A>C
ENST00000475506.1:n.204-117A>C
ENST00000485515.5:n.275-117A>C
ENST00000491274.5:c.245-117A>C	ENSP00000480482.1:n.245-117A>C
NM_003000.2:c.287-117A>C , LRG_316t1:c.287-117A>C	NP_002991.2:n.287-117A>C
NM_003000.3:c.287-117A>C MANE Select	NP_002991.2:n.287-117A>C