Canonical Allele Identifier: CA338227664

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17371259T>A (hg19) ; chr1:g.17044764T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17044764T>A , CM000663.2:g.17044764T>A	GRCh38
NC_000001.10:g.17371259T>A , CM000663.1:g.17371259T>A	GRCh37
NC_000001.9:g.17243846T>A	NCBI36
NG_012340.1:g.14407A>T , LRG_316:g.14407A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.26A>T	ENSP00000481376.2:p.Asn9Ile
ENST00000491274.6:c.155A>T	ENSP00000480482.2:p.Asn52Ile
ENST00000375499.8:c.197A>T MANE Select	ENSP00000364649.3:p.Asn66Ile
ENST00000375499.7:c.197A>T	ENSP00000364649.3:p.Asn66Ile
ENST00000463045.2:c.26A>T	ENSP00000481376.1:p.Asn9Ile
ENST00000466613.2:n.209A>T
ENST00000475506.1:n.114A>T
ENST00000485515.5:n.185A>T
ENST00000491274.5:c.155A>T	ENSP00000480482.1:p.Asn52Ile
NM_003000.2:c.197A>T , LRG_316t1:c.197A>T	NP_002991.2:p.Asn66Ile
NM_003000.3:c.197A>T MANE Select	NP_002991.2:p.Asn66Ile