Canonical Allele Identifier: CA338228366

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17371367T>C (hg19) ; chr1:g.17044872T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17044872T>C , CM000663.2:g.17044872T>C	GRCh38
NC_000001.10:g.17371367T>C , CM000663.1:g.17371367T>C	GRCh37
NC_000001.9:g.17243954T>C	NCBI36
NG_012340.1:g.14299A>G , LRG_316:g.14299A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.-83A>G	ENSP00000481376.2:n.-83A>G
ENST00000491274.6:c.47A>G	ENSP00000480482.2:p.Gln16Arg
ENST00000375499.8:c.89A>G MANE Select	ENSP00000364649.3:p.Gln30Arg
ENST00000375499.7:c.89A>G	ENSP00000364649.3:p.Gln30Arg
ENST00000463045.2:c.-83A>G	ENSP00000481376.1:n.-83A>G
ENST00000466613.2:n.101A>G
ENST00000475506.1:n.6A>G
ENST00000485515.5:n.77A>G
ENST00000491274.5:c.47A>G	ENSP00000480482.1:p.Gln16Arg
NM_003000.2:c.89A>G , LRG_316t1:c.89A>G	NP_002991.2:p.Gln30Arg
NM_003000.3:c.89A>G MANE Select	NP_002991.2:p.Gln30Arg