Canonical Allele Identifier: CA416046995

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17371330A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17044835A>G , CM000663.2:g.17044835A>G	GRCh38
NC_000001.10:g.17371330A>G , CM000663.1:g.17371330A>G	GRCh37
NC_000001.9:g.17243917A>G	NCBI36
NG_012340.1:g.14336T>C , LRG_316:g.14336T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.-46T>C	ENSP00000481376.2:n.-46T>C
ENST00000491274.6:c.84T>C	ENSP00000480482.2:p.Phe28=
ENST00000375499.8:c.126T>C MANE Select	ENSP00000364649.3:p.Phe42=
ENST00000375499.7:c.126T>C	ENSP00000364649.3:p.Phe42=
ENST00000463045.2:c.-46T>C	ENSP00000481376.1:n.-46T>C
ENST00000466613.2:n.138T>C
ENST00000475506.1:n.43T>C
ENST00000485515.5:n.114T>C
ENST00000491274.5:c.84T>C	ENSP00000480482.1:p.Phe28=
NM_003000.2:c.126T>C , LRG_316t1:c.126T>C	NP_002991.2:p.Phe42=
NM_003000.3:c.126T>C MANE Select	NP_002991.2:p.Phe42=