Canonical Allele Identifier: CA089730
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs766038910
gnomAD v2: 1-17349138-G-A
gnomAD v4: 1-17022643-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022643G>A , CM000663.2:g.17022643G>A GRCh38
NC_000001.10:g.17349138G>A , CM000663.1:g.17349138G>A GRCh37
NC_000001.9:g.17221725G>A NCBI36
NG_012340.1:g.36528C>T , LRG_316:g.36528C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.559C>T ENSP00000481376.2:p.His187Tyr
ENST00000491274.6:c.688C>T ENSP00000480482.2:p.His230Tyr
ENST00000375499.8:c.730C>T MANE Select ENSP00000364649.3:p.His244Tyr
ENST00000375499.7:c.730C>T ENSP00000364649.3:p.His244Tyr
ENST00000475049.5:n.155C>T
ENST00000485092.5:n.394C>T
ENST00000485515.5:n.664C>T
NM_003000.2:c.730C>T , LRG_316t1:c.730C>T NP_002991.2:p.His244Tyr
NM_003000.3:c.730C>T MANE Select NP_002991.2:p.His244Tyr