Canonical Allele Identifier: CA2695300631
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs2078101101

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17044904G>A , CM000663.2:g.17044904G>A GRCh38
NC_000001.10:g.17371399G>A , CM000663.1:g.17371399G>A GRCh37
NC_000001.9:g.17243986G>A NCBI36
NG_012340.1:g.14267C>T , LRG_316:g.14267C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.-99-16C>T ENSP00000481376.2:n.-99-16C>T
ENST00000491274.6:c.31-16C>T ENSP00000480482.2:n.31-16C>T
ENST00000375499.8:c.73-16C>T MANE Select ENSP00000364649.3:n.73-16C>T
ENST00000375499.7:c.73-16C>T ENSP00000364649.3:n.73-16C>T
ENST00000463045.2:c.-99-16C>T ENSP00000481376.1:n.-99-16C>T
ENST00000466613.2:n.85-16C>T
ENST00000485515.5:n.61-16C>T
ENST00000491274.5:c.31-16C>T ENSP00000480482.1:n.31-16C>T
NM_003000.2:c.73-16C>T , LRG_316t1:c.73-16C>T NP_002991.2:n.73-16C>T
NM_003000.3:c.73-16C>T MANE Select NP_002991.2:n.73-16C>T