Canonical Allele Identifier: CA338272387

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17354242A>T (hg19) ; chr1:g.17027747A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027747A>T , CM000663.2:g.17027747A>T	GRCh38
NC_000001.10:g.17354242A>T , CM000663.1:g.17354242A>T	GRCh37
NC_000001.9:g.17226829A>T	NCBI36
NG_012340.1:g.31424T>A , LRG_316:g.31424T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.369+2T>A	ENSP00000481376.2:n.369+2T>A
ENST00000491274.6:c.498+2T>A	ENSP00000480482.2:n.498+2T>A
ENST00000375499.8:c.540+2T>A MANE Select	ENSP00000364649.3:n.540+2T>A
ENST00000375499.7:c.540+2T>A	ENSP00000364649.3:n.540+2T>A
ENST00000475506.1:n.459T>A
ENST00000485515.5:n.474+2T>A
ENST00000491274.5:c.498+2T>A	ENSP00000480482.1:n.498+2T>A
NM_003000.2:c.540+2T>A , LRG_316t1:c.540+2T>A	NP_002991.2:n.540+2T>A
NM_003000.3:c.540+2T>A MANE Select	NP_002991.2:n.540+2T>A