Canonical Allele Identifier: CA18666155

Gene: SDHB

Linked Data

• dbSNP Id: rs998376877
• MyVariant Identifiers: chr1:g.17027932T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027932T>G , CM000663.2:g.17027932T>G	GRCh38
NC_000001.10:g.17354427T>G , CM000663.1:g.17354427T>G	GRCh37
NC_000001.9:g.17227014T>G	NCBI36
NG_012340.1:g.31239A>C , LRG_316:g.31239A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.253-67A>C	ENSP00000481376.2:n.253-67A>C
ENST00000491274.6:c.382-67A>C	ENSP00000480482.2:n.382-67A>C
ENST00000375499.8:c.424-67A>C MANE Select	ENSP00000364649.3:n.424-67A>C
ENST00000375499.7:c.424-67A>C	ENSP00000364649.3:n.424-67A>C
ENST00000463045.2:c.253-67A>C	ENSP00000481376.1:n.253-67A>C
ENST00000475506.1:n.341-67A>C
ENST00000485515.5:n.358-67A>C
ENST00000491274.5:c.382-67A>C	ENSP00000480482.1:n.382-67A>C
NM_003000.2:c.424-67A>C , LRG_316t1:c.424-67A>C	NP_002991.2:n.424-67A>C
NM_003000.3:c.424-67A>C MANE Select	NP_002991.2:n.424-67A>C