Canonical Allele Identifier: CA338275157

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17355222C>G (hg19) ; chr1:g.17028727C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17028727C>G , CM000663.2:g.17028727C>G	GRCh38
NC_000001.10:g.17355222C>G , CM000663.1:g.17355222C>G	GRCh37
NC_000001.9:g.17227809C>G	NCBI36
NG_012340.1:g.30444G>C , LRG_316:g.30444G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.125G>C	ENSP00000481376.2:p.Gly42Ala
ENST00000491274.6:c.254G>C	ENSP00000480482.2:p.Gly85Ala
ENST00000375499.8:c.296G>C MANE Select	ENSP00000364649.3:p.Gly99Ala
ENST00000375499.7:c.296G>C	ENSP00000364649.3:p.Gly99Ala
ENST00000463045.2:c.125G>C	ENSP00000481376.1:p.Gly42Ala
ENST00000475506.1:n.213G>C
ENST00000485515.5:n.284G>C
ENST00000491274.5:c.254G>C	ENSP00000480482.1:p.Gly85Ala
NM_003000.2:c.296G>C , LRG_316t1:c.296G>C	NP_002991.2:p.Gly99Ala
NM_003000.3:c.296G>C MANE Select	NP_002991.2:p.Gly99Ala