Canonical Allele Identifier: CA890972308

Gene: SDHB

Linked Data

• dbSNP Id: rs1326638022
• gnomAD v3: 1-17028152-A-G
• gnomAD v4: 1-17028152-A-G
• MyVariant Identifiers: chr1:g.17354647A>G (hg19) ; chr1:g.17028152A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17028152A>G , CM000663.2:g.17028152A>G	GRCh38
NC_000001.10:g.17354647A>G , CM000663.1:g.17354647A>G	GRCh37
NC_000001.9:g.17227234A>G	NCBI36
NG_012340.1:g.31019T>C , LRG_316:g.31019T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.253-287T>C	ENSP00000481376.2:n.253-287T>C
ENST00000491274.6:c.382-287T>C	ENSP00000480482.2:n.382-287T>C
ENST00000375499.8:c.424-287T>C MANE Select	ENSP00000364649.3:n.424-287T>C
ENST00000375499.7:c.424-287T>C	ENSP00000364649.3:n.424-287T>C
ENST00000463045.2:c.253-287T>C	ENSP00000481376.1:n.253-287T>C
ENST00000475506.1:n.341-287T>C
ENST00000485515.5:n.358-287T>C
ENST00000491274.5:c.382-287T>C	ENSP00000480482.1:n.382-287T>C
NM_003000.2:c.424-287T>C , LRG_316t1:c.424-287T>C	NP_002991.2:n.424-287T>C
NM_003000.3:c.424-287T>C MANE Select	NP_002991.2:n.424-287T>C