Canonical Allele Identifier: CA338270035

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17349121G>C (hg19) ; chr1:g.17022626G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17022626G>C , CM000663.2:g.17022626G>C	GRCh38
NC_000001.10:g.17349121G>C , CM000663.1:g.17349121G>C	GRCh37
NC_000001.9:g.17221708G>C	NCBI36
NG_012340.1:g.36545C>G , LRG_316:g.36545C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.576C>G	ENSP00000481376.2:p.Cys192Trp
ENST00000491274.6:c.705C>G	ENSP00000480482.2:p.Cys235Trp
ENST00000375499.8:c.747C>G MANE Select	ENSP00000364649.3:p.Cys249Trp
ENST00000375499.7:c.747C>G	ENSP00000364649.3:p.Cys249Trp
ENST00000475049.5:n.172C>G
ENST00000485092.5:n.411C>G
ENST00000485515.5:n.681C>G
NM_003000.2:c.747C>G , LRG_316t1:c.747C>G	NP_002991.2:p.Cys249Trp
NM_003000.3:c.747C>G MANE Select	NP_002991.2:p.Cys249Trp