Canonical Allele Identifier: CA416085630
Gene: SDHB HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.17354246G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17027751G>A , CM000663.2:g.17027751G>A GRCh38
NC_000001.10:g.17354246G>A , CM000663.1:g.17354246G>A GRCh37
NC_000001.9:g.17226833G>A NCBI36
NG_012340.1:g.31420C>T , LRG_316:g.31420C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.367C>T ENSP00000481376.2:p.Leu123=
ENST00000491274.6:c.496C>T ENSP00000480482.2:p.Leu166=
ENST00000375499.8:c.538C>T MANE Select ENSP00000364649.3:p.Leu180=
ENST00000375499.7:c.538C>T ENSP00000364649.3:p.Leu180=
ENST00000463045.2:c.367C>T ENSP00000481376.1:p.Leu123=
ENST00000475506.1:n.455C>T
ENST00000485515.5:n.472C>T
ENST00000491274.5:c.496C>T ENSP00000480482.1:p.Leu166=
NM_003000.2:c.538C>T , LRG_316t1:c.538C>T NP_002991.2:p.Leu180=
NM_003000.3:c.538C>T MANE Select NP_002991.2:p.Leu180=