Canonical Allele Identifier: CA999084712

Gene: SDHB

Linked Data

• dbSNP Id: rs2078006201
• gnomAD v3: 1-17028847-G-C
• gnomAD v4: 1-17028847-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17028847G>C , CM000663.2:g.17028847G>C	GRCh38
NC_000001.10:g.17355342G>C , CM000663.1:g.17355342G>C	GRCh37
NC_000001.9:g.17227929G>C	NCBI36
NG_012340.1:g.30324C>G , LRG_316:g.30324C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.116-111C>G	ENSP00000481376.2:n.116-111C>G
ENST00000491274.6:c.245-111C>G	ENSP00000480482.2:n.245-111C>G
ENST00000375499.8:c.287-111C>G MANE Select	ENSP00000364649.3:n.287-111C>G
ENST00000375499.7:c.287-111C>G	ENSP00000364649.3:n.287-111C>G
ENST00000463045.2:c.116-111C>G	ENSP00000481376.1:n.116-111C>G
ENST00000475506.1:n.204-111C>G
ENST00000485515.5:n.275-111C>G
ENST00000491274.5:c.245-111C>G	ENSP00000480482.1:n.245-111C>G
NM_003000.2:c.287-111C>G , LRG_316t1:c.287-111C>G	NP_002991.2:n.287-111C>G
NM_003000.3:c.287-111C>G MANE Select	NP_002991.2:n.287-111C>G