Canonical Allele Identifier: CA338270061

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17349125T>A (hg19) ; chr1:g.17022630T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17022630T>A , CM000663.2:g.17022630T>A	GRCh38
NC_000001.10:g.17349125T>A , CM000663.1:g.17349125T>A	GRCh37
NC_000001.9:g.17221712T>A	NCBI36
NG_012340.1:g.36541A>T , LRG_316:g.36541A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.572A>T	ENSP00000481376.2:p.Asn191Ile
ENST00000491274.6:c.701A>T	ENSP00000480482.2:p.Asn234Ile
ENST00000375499.8:c.743A>T MANE Select	ENSP00000364649.3:p.Asn248Ile
ENST00000375499.7:c.743A>T	ENSP00000364649.3:p.Asn248Ile
ENST00000475049.5:n.168A>T
ENST00000485092.5:n.407A>T
ENST00000485515.5:n.677A>T
NM_003000.2:c.743A>T , LRG_316t1:c.743A>T	NP_002991.2:p.Asn248Ile
NM_003000.3:c.743A>T MANE Select	NP_002991.2:p.Asn248Ile