Canonical Allele Identifier: CA338227704

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17371263G>T (hg19) ; chr1:g.17044768G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17044768G>T , CM000663.2:g.17044768G>T	GRCh38
NC_000001.10:g.17371263G>T , CM000663.1:g.17371263G>T	GRCh37
NC_000001.9:g.17243850G>T	NCBI36
NG_012340.1:g.14403C>A , LRG_316:g.14403C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.22C>A	ENSP00000481376.2:p.Leu8Ile
ENST00000491274.6:c.151C>A	ENSP00000480482.2:p.Leu51Ile
ENST00000375499.8:c.193C>A MANE Select	ENSP00000364649.3:p.Leu65Ile
ENST00000375499.7:c.193C>A	ENSP00000364649.3:p.Leu65Ile
ENST00000463045.2:c.22C>A	ENSP00000481376.1:p.Leu8Ile
ENST00000466613.2:n.205C>A
ENST00000475506.1:n.110C>A
ENST00000485515.5:n.181C>A
ENST00000491274.5:c.151C>A	ENSP00000480482.1:p.Leu51Ile
NM_003000.2:c.193C>A , LRG_316t1:c.193C>A	NP_002991.2:p.Leu65Ile
NM_003000.3:c.193C>A MANE Select	NP_002991.2:p.Leu65Ile