Canonical Allele Identifier: CA2615982784
Gene: SDHD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112086863A>G , CM000673.2:g.112086863A>G GRCh38
NC_000011.9:g.111957587A>G , CM000673.1:g.111957587A>G GRCh37
NC_000011.8:g.111462797A>G NCBI36
NG_012337.2:g.5017A>G
NG_033145.1:g.4936T>C
NG_012337.3:g.5017A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000640554.1:c.-45A>G ENSP00000491141.1:n.-45A>G
ENST00000375549.7:c.-45A>G ENSP00000364699.3:n.-45A>G
ENST00000614349.4:c.-45A>G ENSP00000480666.1:n.-45A>G
NM_001276503.1:c.-45A>G NP_001263432.1:n.-45A>G
NM_001276504.1:c.-45A>G NP_001263433.1:n.-45A>G
NM_001276506.1:c.-45A>G NP_001263435.1:n.-45A>G
NM_003002.3:c.-45A>G NP_002993.1:n.-45A>G
NR_077060.1:n.40A>G