Canonical Allele Identifier: CA338227609

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17371254A>G (hg19) ; chr1:g.17044759A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17044759A>G , CM000663.2:g.17044759A>G	GRCh38
NC_000001.10:g.17371254A>G , CM000663.1:g.17371254A>G	GRCh37
NC_000001.9:g.17243841A>G	NCBI36
NG_012340.1:g.14412T>C , LRG_316:g.14412T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.29+2T>C	ENSP00000481376.2:n.29+2T>C
ENST00000491274.6:c.158+2T>C	ENSP00000480482.2:n.158+2T>C
ENST00000375499.8:c.200+2T>C MANE Select	ENSP00000364649.3:n.200+2T>C
ENST00000375499.7:c.200+2T>C	ENSP00000364649.3:n.200+2T>C
ENST00000463045.2:c.29+2T>C	ENSP00000481376.1:n.29+2T>C
ENST00000466613.2:n.212+2T>C
ENST00000475506.1:n.117+2T>C
ENST00000485515.5:n.188+2T>C
ENST00000491274.5:c.158+2T>C	ENSP00000480482.1:n.158+2T>C
NM_003000.2:c.200+2T>C , LRG_316t1:c.200+2T>C	NP_002991.2:n.200+2T>C
NM_003000.3:c.200+2T>C MANE Select	NP_002991.2:n.200+2T>C