Canonical Allele Identifier: CA2724941476
Gene: SDHD HGNC NCBI

Linked Data

dbSNP Id: rs372894110

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112086888C>T , CM000673.2:g.112086888C>T GRCh38
NC_000011.9:g.111957612C>T , CM000673.1:g.111957612C>T GRCh37
NC_000011.8:g.111462822C>T NCBI36
NG_012337.2:g.5042C>T
NG_033145.1:g.4911G>A
NG_012337.3:g.5042C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000530923.6:c.-20C>T ENSP00000432946.2:n.-20C>T
ENST00000534010.2:c.-20C>T ENSP00000433202.2:n.-20C>T
ENST00000375549.8:c.-20C>T MANE Select ENSP00000364699.3:n.-20C>T
ENST00000528021.6:c.-20C>T ENSP00000432465.1:n.-20C>T
ENST00000640554.1:c.-20C>T ENSP00000491141.1:n.-20C>T
ENST00000375549.7:c.-20C>T ENSP00000364699.3:n.-20C>T
ENST00000528021.5:c.-20C>T ENSP00000432465.1:n.-20C>T
ENST00000528048.5:c.-20C>T ENSP00000436217.1:n.-20C>T
ENST00000528182.5:c.-20C>T ENSP00000435475.1:n.-20C>T
ENST00000614349.4:c.-20C>T ENSP00000480666.1:n.-20C>T
NM_001276503.1:c.-20C>T NP_001263432.1:n.-20C>T
NM_001276504.1:c.-20C>T NP_001263433.1:n.-20C>T
NM_001276506.1:c.-20C>T NP_001263435.1:n.-20C>T
NM_003002.3:c.-20C>T NP_002993.1:n.-20C>T
NR_077060.1:n.65C>T
NM_003002.4:c.-20C>T MANE Select NP_002993.1:n.-20C>T
NM_001276503.2:c.-20C>T NP_001263432.1:n.-20C>T
NM_001276504.2:c.-20C>T NP_001263433.1:n.-20C>T
NM_001276506.2:c.-20C>T NP_001263435.1:n.-20C>T
NR_077060.2:n.16C>T