Canonical Allele Identifier: CA2000559475
Gene: SDHD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112086837G= , CM000673.2:g.112086837G= GRCh38
NC_000011.9:g.111957561G= , CM000673.1:g.111957561G= GRCh37
NC_000011.8:g.111462771G= NCBI36
NG_012337.2:g.4991G=
NG_033145.1:g.4962C=
NG_012337.3:g.4991G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000640554.1:c.-71G= ENSP00000491141.1:n.-71G=
ENST00000375549.7:c.-71G= ENSP00000364699.3:n.-71G=
ENST00000614349.4:c.-71G= ENSP00000480666.1:n.-71G=
NM_001276503.1:c.-71G= NP_001263432.1:n.-71G=
NM_001276504.1:c.-71G= NP_001263433.1:n.-71G=
NM_001276506.1:c.-71G= NP_001263435.1:n.-71G=
NM_003002.3:c.-71G= NP_002993.1:n.-71G=
NR_077060.1:n.14G=