Canonical Allele Identifier: CA1156077988
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022651T= , CM000663.2:g.17022651T= GRCh38
NC_000001.10:g.17349146T= , CM000663.1:g.17349146T= GRCh37
NC_000001.9:g.17221733T= NCBI36
NG_012340.1:g.36520A= , LRG_316:g.36520A=

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.551A= ENSP00000481376.2:p.Tyr184=
ENST00000491274.6:c.680A= ENSP00000480482.2:p.Tyr227=
ENST00000375499.8:c.722A= MANE Select ENSP00000364649.3:p.Tyr241=
ENST00000375499.7:c.722A= ENSP00000364649.3:p.Tyr241=
ENST00000475049.5:n.147A=
ENST00000485092.5:n.386A=
ENST00000485515.5:n.656A=
NM_003000.2:c.722A= , LRG_316t1:c.722A= NP_002991.2:p.Tyr241=
NM_003000.3:c.722A= MANE Select NP_002991.2:p.Tyr241=