Canonical Allele Identifier: CA338272620

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17354278T>G (hg19) ; chr1:g.17027783T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027783T>G , CM000663.2:g.17027783T>G	GRCh38
NC_000001.10:g.17354278T>G , CM000663.1:g.17354278T>G	GRCh37
NC_000001.9:g.17226865T>G	NCBI36
NG_012340.1:g.31388A>C , LRG_316:g.31388A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.335A>C	ENSP00000481376.2:p.Gln112Pro
ENST00000491274.6:c.464A>C	ENSP00000480482.2:p.Gln155Pro
ENST00000375499.8:c.506A>C MANE Select	ENSP00000364649.3:p.Gln169Pro
ENST00000375499.7:c.506A>C	ENSP00000364649.3:p.Gln169Pro
ENST00000463045.2:c.335A>C	ENSP00000481376.1:p.Gln112Pro
ENST00000475506.1:n.423A>C
ENST00000485515.5:n.440A>C
ENST00000491274.5:c.464A>C	ENSP00000480482.1:p.Gln155Pro
NM_003000.2:c.506A>C , LRG_316t1:c.506A>C	NP_002991.2:p.Gln169Pro
NM_003000.3:c.506A>C MANE Select	NP_002991.2:p.Gln169Pro