Canonical Allele Identifier: CA416085618
Gene: SDHB HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.17354244C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17027749C>G , CM000663.2:g.17027749C>G GRCh38
NC_000001.10:g.17354244C>G , CM000663.1:g.17354244C>G GRCh37
NC_000001.9:g.17226831C>G NCBI36
NG_012340.1:g.31422G>C , LRG_316:g.31422G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.369G>C ENSP00000481376.2:p.Leu123=
ENST00000491274.6:c.498G>C ENSP00000480482.2:p.Leu166=
ENST00000375499.8:c.540G>C MANE Select ENSP00000364649.3:p.Leu180=
ENST00000375499.7:c.540G>C ENSP00000364649.3:p.Leu180=
ENST00000463045.2:c.369G>C ENSP00000481376.1:p.Leu123=
ENST00000475506.1:n.457G>C
ENST00000485515.5:n.474G>C
ENST00000491274.5:c.498G>C ENSP00000480482.1:p.Leu166=
NM_003000.2:c.540G>C , LRG_316t1:c.540G>C NP_002991.2:p.Leu180=
NM_003000.3:c.540G>C MANE Select NP_002991.2:p.Leu180=