Canonical Allele Identifier: CA338276573

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17359605A>T (hg19) ; chr1:g.17033110A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17033110A>T , CM000663.2:g.17033110A>T	GRCh38
NC_000001.10:g.17359605A>T , CM000663.1:g.17359605A>T	GRCh37
NC_000001.9:g.17232192A>T	NCBI36
NG_012340.1:g.26061T>A , LRG_316:g.26061T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.65T>A	ENSP00000481376.2:p.Ile22Asn
ENST00000491274.6:c.194T>A	ENSP00000480482.2:p.Ile65Asn
ENST00000375499.8:c.236T>A MANE Select	ENSP00000364649.3:p.Ile79Asn
ENST00000375499.7:c.236T>A	ENSP00000364649.3:p.Ile79Asn
ENST00000463045.2:c.65T>A	ENSP00000481376.1:p.Ile22Asn
ENST00000466613.2:n.248T>A
ENST00000475506.1:n.153T>A
ENST00000485515.5:n.224T>A
ENST00000491274.5:c.194T>A	ENSP00000480482.1:p.Ile65Asn
NM_003000.2:c.236T>A , LRG_316t1:c.236T>A	NP_002991.2:p.Ile79Asn
NM_003000.3:c.236T>A MANE Select	NP_002991.2:p.Ile79Asn