Canonical Allele Identifier: CA2695453776
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs2101513321

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022527G>A , CM000663.2:g.17022527G>A GRCh38
NC_000001.10:g.17349022G>A , CM000663.1:g.17349022G>A GRCh37
NC_000001.9:g.17221609G>A NCBI36
NG_012340.1:g.36644C>T , LRG_316:g.36644C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.594+81C>T ENSP00000481376.2:n.594+81C>T
ENST00000491274.6:c.723+81C>T ENSP00000480482.2:n.723+81C>T
ENST00000375499.8:c.765+81C>T MANE Select ENSP00000364649.3:n.765+81C>T
ENST00000375499.7:c.765+81C>T ENSP00000364649.3:n.765+81C>T
ENST00000475049.5:n.190+81C>T
ENST00000485092.5:n.429+81C>T
NM_003000.2:c.765+81C>T , LRG_316t1:c.765+81C>T NP_002991.2:n.765+81C>T
NM_003000.3:c.765+81C>T MANE Select NP_002991.2:n.765+81C>T