Canonical Allele Identifier: CA338270028

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17349120T>A (hg19) ; chr1:g.17022625T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17022625T>A , CM000663.2:g.17022625T>A	GRCh38
NC_000001.10:g.17349120T>A , CM000663.1:g.17349120T>A	GRCh37
NC_000001.9:g.17221707T>A	NCBI36
NG_012340.1:g.36546A>T , LRG_316:g.36546A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.577A>T	ENSP00000481376.2:p.Thr193Ser
ENST00000491274.6:c.706A>T	ENSP00000480482.2:p.Thr236Ser
ENST00000375499.8:c.748A>T MANE Select	ENSP00000364649.3:p.Thr250Ser
ENST00000375499.7:c.748A>T	ENSP00000364649.3:p.Thr250Ser
ENST00000475049.5:n.173A>T
ENST00000485092.5:n.412A>T
ENST00000485515.5:n.682A>T
NM_003000.2:c.748A>T , LRG_316t1:c.748A>T	NP_002991.2:p.Thr250Ser
NM_003000.3:c.748A>T MANE Select	NP_002991.2:p.Thr250Ser