Canonical Allele Identifier: CA2000561894
Gene: SDHD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112088906G= , CM000673.2:g.112088906G= GRCh38
NC_000011.9:g.111959630G= , CM000673.1:g.111959630G= GRCh37
NC_000011.8:g.111464840G= NCBI36
NG_012337.2:g.7060G=
NG_033145.1:g.2893C=
NG_012337.3:g.7060G=

Transcript Alleles

HGVS Amino-acid change
ENST00000530923.6:c.209G= ENSP00000432946.2:p.Arg70=
ENST00000534010.2:c.209G= ENSP00000433202.2:p.Arg70=
ENST00000375549.8:c.209G= MANE Select ENSP00000364699.3:p.Arg70=
ENST00000528021.6:c.209G= ENSP00000432465.1:p.Arg70=
ENST00000640554.1:c.*281G= ENSP00000491141.1:n.*281G=
ENST00000375549.7:c.209G= ENSP00000364699.3:p.Arg70=
ENST00000525291.5:c.92G= ENSP00000436669.1:p.Arg31=
ENST00000525987.5:n.214G=
ENST00000526592.5:c.209G= ENSP00000432005.1:p.Arg70=
ENST00000528021.5:c.209G= ENSP00000432465.1:p.Arg70=
ENST00000528048.5:c.169+933G= ENSP00000436217.1:n.169+933G=
ENST00000528182.5:c.209G= ENSP00000435475.1:p.Arg70=
ENST00000530923.5:c.199G=
ENST00000531744.5:c.209G= ENSP00000456957.1:p.Arg70=
ENST00000532699.1:c.209G= ENSP00000456434.1:p.Arg70=
ENST00000534010.1:c.40G=
ENST00000614349.4:c.209G= ENSP00000480666.1:p.Arg70=
NM_001276503.1:c.169+933G= NP_001263432.1:n.169+933G=
NM_001276504.1:c.92G= NP_001263433.1:p.Arg31=
NM_001276506.1:c.209G= NP_001263435.1:p.Arg70=
NM_003002.3:c.209G= NP_002993.1:p.Arg70=
NR_077060.1:n.293G=
NM_003002.4:c.209G= MANE Select NP_002993.1:p.Arg70=
NM_001276503.2:c.169+933G= NP_001263432.1:n.169+933G=
NM_001276504.2:c.92G= NP_001263433.1:p.Arg31=
NM_001276506.2:c.209G= NP_001263435.1:p.Arg70=
NR_077060.2:n.244G=