Canonical Allele Identifier: CA2643679656

Gene: SDHB

Linked Data

• gnomAD v4: 1-17044895-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17044895T>C , CM000663.2:g.17044895T>C	GRCh38
NC_000001.10:g.17371390T>C , CM000663.1:g.17371390T>C	GRCh37
NC_000001.9:g.17243977T>C	NCBI36
NG_012340.1:g.14276A>G , LRG_316:g.14276A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.-99-7A>G	ENSP00000481376.2:n.-99-7A>G
ENST00000491274.6:c.31-7A>G	ENSP00000480482.2:n.31-7A>G
ENST00000375499.8:c.73-7A>G MANE Select	ENSP00000364649.3:n.73-7A>G
ENST00000375499.7:c.73-7A>G	ENSP00000364649.3:n.73-7A>G
ENST00000463045.2:c.-99-7A>G	ENSP00000481376.1:n.-99-7A>G
ENST00000466613.2:n.85-7A>G
ENST00000485515.5:n.61-7A>G
ENST00000491274.5:c.31-7A>G	ENSP00000480482.1:n.31-7A>G
NM_003000.2:c.73-7A>G , LRG_316t1:c.73-7A>G	NP_002991.2:n.73-7A>G
NM_003000.3:c.73-7A>G MANE Select	NP_002991.2:n.73-7A>G