Canonical Allele Identifier: CA338272490

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17354256C>A (hg19) ; chr1:g.17027761C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027761C>A , CM000663.2:g.17027761C>A	GRCh38
NC_000001.10:g.17354256C>A , CM000663.1:g.17354256C>A	GRCh37
NC_000001.9:g.17226843C>A	NCBI36
NG_012340.1:g.31410G>T , LRG_316:g.31410G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.357G>T	ENSP00000481376.2:p.Glu119Asp
ENST00000491274.6:c.486G>T	ENSP00000480482.2:p.Glu162Asp
ENST00000375499.8:c.528G>T MANE Select	ENSP00000364649.3:p.Glu176Asp
ENST00000375499.7:c.528G>T	ENSP00000364649.3:p.Glu176Asp
ENST00000463045.2:c.357G>T	ENSP00000481376.1:p.Glu119Asp
ENST00000475506.1:n.445G>T
ENST00000485515.5:n.462G>T
ENST00000491274.5:c.486G>T	ENSP00000480482.1:p.Glu162Asp
NM_003000.2:c.528G>T , LRG_316t1:c.528G>T	NP_002991.2:p.Glu176Asp
NM_003000.3:c.528G>T MANE Select	NP_002991.2:p.Glu176Asp