Canonical Allele Identifier: CA2000559489
Gene: SDHD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112086843G= , CM000673.2:g.112086843G= GRCh38
NC_000011.9:g.111957567G= , CM000673.1:g.111957567G= GRCh37
NC_000011.8:g.111462777G= NCBI36
NG_012337.2:g.4997G=
NG_033145.1:g.4956C=
NG_012337.3:g.4997G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000640554.1:c.-65G= ENSP00000491141.1:n.-65G=
ENST00000375549.7:c.-65G= ENSP00000364699.3:n.-65G=
ENST00000614349.4:c.-65G= ENSP00000480666.1:n.-65G=
NM_001276503.1:c.-65G= NP_001263432.1:n.-65G=
NM_001276504.1:c.-65G= NP_001263433.1:n.-65G=
NM_001276506.1:c.-65G= NP_001263435.1:n.-65G=
NM_003002.3:c.-65G= NP_002993.1:n.-65G=
NR_077060.1:n.20G=