Canonical Allele Identifier: CA2615982819
Gene: SDHD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112086897T>A , CM000673.2:g.112086897T>A GRCh38
NC_000011.9:g.111957621T>A , CM000673.1:g.111957621T>A GRCh37
NC_000011.8:g.111462831T>A NCBI36
NG_012337.2:g.5051T>A
NG_033145.1:g.4902A>T
NG_012337.3:g.5051T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000530923.6:c.-11T>A ENSP00000432946.2:n.-11T>A
ENST00000534010.2:c.-11T>A ENSP00000433202.2:n.-11T>A
ENST00000375549.8:c.-11T>A MANE Select ENSP00000364699.3:n.-11T>A
ENST00000528021.6:c.-11T>A ENSP00000432465.1:n.-11T>A
ENST00000640554.1:c.-11T>A ENSP00000491141.1:n.-11T>A
ENST00000375549.7:c.-11T>A ENSP00000364699.3:n.-11T>A
ENST00000528021.5:c.-11T>A ENSP00000432465.1:n.-11T>A
ENST00000528048.5:c.-11T>A ENSP00000436217.1:n.-11T>A
ENST00000528182.5:c.-11T>A ENSP00000435475.1:n.-11T>A
ENST00000614349.4:c.-11T>A ENSP00000480666.1:n.-11T>A
NM_001276503.1:c.-11T>A NP_001263432.1:n.-11T>A
NM_001276504.1:c.-11T>A NP_001263433.1:n.-11T>A
NM_001276506.1:c.-11T>A NP_001263435.1:n.-11T>A
NM_003002.3:c.-11T>A NP_002993.1:n.-11T>A
NR_077060.1:n.74T>A
NM_003002.4:c.-11T>A MANE Select NP_002993.1:n.-11T>A
NM_001276503.2:c.-11T>A NP_001263432.1:n.-11T>A
NM_001276504.2:c.-11T>A NP_001263433.1:n.-11T>A
NM_001276506.2:c.-11T>A NP_001263435.1:n.-11T>A
NR_077060.2:n.25T>A