Canonical Allele Identifier: CA416046947

Gene: SDHB

Linked Data

• dbSNP Id: rs1351034939
• gnomAD v2: 1-17371321-A-G
• gnomAD v4: 1-17044826-A-G
• MyVariant Identifiers: chr1:g.17371321A>G (hg19) ; chr1:g.17044826A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17044826A>G , CM000663.2:g.17044826A>G	GRCh38
NC_000001.10:g.17371321A>G , CM000663.1:g.17371321A>G	GRCh37
NC_000001.9:g.17243908A>G	NCBI36
NG_012340.1:g.14345T>C , LRG_316:g.14345T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.-37T>C	ENSP00000481376.2:n.-37T>C
ENST00000491274.6:c.93T>C	ENSP00000480482.2:p.Tyr31=
ENST00000375499.8:c.135T>C MANE Select	ENSP00000364649.3:p.Tyr45=
ENST00000375499.7:c.135T>C	ENSP00000364649.3:p.Tyr45=
ENST00000463045.2:c.-37T>C	ENSP00000481376.1:n.-37T>C
ENST00000466613.2:n.147T>C
ENST00000475506.1:n.52T>C
ENST00000485515.5:n.123T>C
ENST00000491274.5:c.93T>C	ENSP00000480482.1:p.Tyr31=
NM_003000.2:c.135T>C , LRG_316t1:c.135T>C	NP_002991.2:p.Tyr45=
NM_003000.3:c.135T>C MANE Select	NP_002991.2:p.Tyr45=