Canonical Allele Identifier: CA338273461

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17354351T>C (hg19) ; chr1:g.17027856T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027856T>C , CM000663.2:g.17027856T>C	GRCh38
NC_000001.10:g.17354351T>C , CM000663.1:g.17354351T>C	GRCh37
NC_000001.9:g.17226938T>C	NCBI36
NG_012340.1:g.31315A>G , LRG_316:g.31315A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.262A>G	ENSP00000481376.2:p.Asn88Asp
ENST00000491274.6:c.391A>G	ENSP00000480482.2:p.Asn131Asp
ENST00000375499.8:c.433A>G MANE Select	ENSP00000364649.3:p.Asn145Asp
ENST00000375499.7:c.433A>G	ENSP00000364649.3:p.Asn145Asp
ENST00000463045.2:c.262A>G	ENSP00000481376.1:p.Asn88Asp
ENST00000475506.1:n.350A>G
ENST00000485515.5:n.367A>G
ENST00000491274.5:c.391A>G	ENSP00000480482.1:p.Asn131Asp
NM_003000.2:c.433A>G , LRG_316t1:c.433A>G	NP_002991.2:p.Asn145Asp
NM_003000.3:c.433A>G MANE Select	NP_002991.2:p.Asn145Asp