Canonical Allele Identifier: CA338228187

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17371331A>C (hg19) ; chr1:g.17044836A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17044836A>C , CM000663.2:g.17044836A>C	GRCh38
NC_000001.10:g.17371331A>C , CM000663.1:g.17371331A>C	GRCh37
NC_000001.9:g.17243918A>C	NCBI36
NG_012340.1:g.14335T>G , LRG_316:g.14335T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.-47T>G	ENSP00000481376.2:n.-47T>G
ENST00000491274.6:c.83T>G	ENSP00000480482.2:p.Phe28Cys
ENST00000375499.8:c.125T>G MANE Select	ENSP00000364649.3:p.Phe42Cys
ENST00000375499.7:c.125T>G	ENSP00000364649.3:p.Phe42Cys
ENST00000463045.2:c.-47T>G	ENSP00000481376.1:n.-47T>G
ENST00000466613.2:n.137T>G
ENST00000475506.1:n.42T>G
ENST00000485515.5:n.113T>G
ENST00000491274.5:c.83T>G	ENSP00000480482.1:p.Phe28Cys
NM_003000.2:c.125T>G , LRG_316t1:c.125T>G	NP_002991.2:p.Phe42Cys
NM_003000.3:c.125T>G MANE Select	NP_002991.2:p.Phe42Cys