Canonical Allele Identifier: CA1156091348

Gene: SDHB

Linked Data

• dbSNP Id: rs2078101264
• gnomAD v4: 1-17044906-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17044906T>C , CM000663.2:g.17044906T>C	GRCh38
NC_000001.10:g.17371401T>C , CM000663.1:g.17371401T>C	GRCh37
NC_000001.9:g.17243988T>C	NCBI36
NG_012340.1:g.14265A>G , LRG_316:g.14265A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.-99-18A>G	ENSP00000481376.2:n.-99-18A>G
ENST00000491274.6:c.31-18A>G	ENSP00000480482.2:n.31-18A>G
ENST00000375499.8:c.73-18A>G MANE Select	ENSP00000364649.3:n.73-18A>G
ENST00000375499.7:c.73-18A>G	ENSP00000364649.3:n.73-18A>G
ENST00000463045.2:c.-99-18A>G	ENSP00000481376.1:n.-99-18A>G
ENST00000466613.2:n.85-18A>G
ENST00000485515.5:n.61-18A>G
ENST00000491274.5:c.31-18A>G	ENSP00000480482.1:n.31-18A>G
NM_003000.2:c.73-18A>G , LRG_316t1:c.73-18A>G	NP_002991.2:n.73-18A>G
NM_003000.3:c.73-18A>G MANE Select	NP_002991.2:n.73-18A>G