Canonical Allele Identifier: CA1156077942
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022554T= , CM000663.2:g.17022554T= GRCh38
NC_000001.10:g.17349049T= , CM000663.1:g.17349049T= GRCh37
NC_000001.9:g.17221636T= NCBI36
NG_012340.1:g.36617A= , LRG_316:g.36617A=

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.594+54A= ENSP00000481376.2:n.594+54A=
ENST00000491274.6:c.723+54A= ENSP00000480482.2:n.723+54A=
ENST00000375499.8:c.765+54A= MANE Select ENSP00000364649.3:n.765+54A=
ENST00000375499.7:c.765+54A= ENSP00000364649.3:n.765+54A=
ENST00000475049.5:n.190+54A=
ENST00000485092.5:n.429+54A=
NM_003000.2:c.765+54A= , LRG_316t1:c.765+54A= NP_002991.2:n.765+54A=
NM_003000.3:c.765+54A= MANE Select NP_002991.2:n.765+54A=