Canonical Allele Identifier: CA338276575

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17359606T>C (hg19) ; chr1:g.17033111T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17033111T>C , CM000663.2:g.17033111T>C	GRCh38
NC_000001.10:g.17359606T>C , CM000663.1:g.17359606T>C	GRCh37
NC_000001.9:g.17232193T>C	NCBI36
NG_012340.1:g.26060A>G , LRG_316:g.26060A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.64A>G	ENSP00000481376.2:p.Ile22Val
ENST00000491274.6:c.193A>G	ENSP00000480482.2:p.Ile65Val
ENST00000375499.8:c.235A>G MANE Select	ENSP00000364649.3:p.Ile79Val
ENST00000375499.7:c.235A>G	ENSP00000364649.3:p.Ile79Val
ENST00000463045.2:c.64A>G	ENSP00000481376.1:p.Ile22Val
ENST00000466613.2:n.247A>G
ENST00000475506.1:n.152A>G
ENST00000485515.5:n.223A>G
ENST00000491274.5:c.193A>G	ENSP00000480482.1:p.Ile65Val
NM_003000.2:c.235A>G , LRG_316t1:c.235A>G	NP_002991.2:p.Ile79Val
NM_003000.3:c.235A>G MANE Select	NP_002991.2:p.Ile79Val