Canonical Allele Identifier: CA416081899
Gene: SDHB HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.17349148T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022653T>A , CM000663.2:g.17022653T>A GRCh38
NC_000001.10:g.17349148T>A , CM000663.1:g.17349148T>A GRCh37
NC_000001.9:g.17221735T>A NCBI36
NG_012340.1:g.36518A>T , LRG_316:g.36518A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.549A>T ENSP00000481376.2:p.Leu183=
ENST00000491274.6:c.678A>T ENSP00000480482.2:p.Leu226=
ENST00000375499.8:c.720A>T MANE Select ENSP00000364649.3:p.Leu240=
ENST00000375499.7:c.720A>T ENSP00000364649.3:p.Leu240=
ENST00000475049.5:n.145A>T
ENST00000485092.5:n.384A>T
ENST00000485515.5:n.654A>T
NM_003000.2:c.720A>T , LRG_316t1:c.720A>T NP_002991.2:p.Leu240=
NM_003000.3:c.720A>T MANE Select NP_002991.2:p.Leu240=