Canonical Allele Identifier: CA10582865
Gene: SDHD HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 239460
ClinVar RCV Id: RCV000232971
dbSNP Id: rs878854589

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112086917dup , CM000673.2:g.112086917dup GRCh38
NC_000011.9:g.111957641dup , CM000673.1:g.111957641dup GRCh37
NC_000011.8:g.111462851dup NCBI36
NG_012337.2:g.5071dup
NG_033145.1:g.4882dup
NG_012337.3:g.5071dup

Transcript Alleles

HGVS Amino-acid change
NM_001276503.1:c.10dup VV
NM_001276504.1:c.10dup VV
NM_001276506.1:c.10dup VV
NM_003002.3:c.10dup VV
NR_077060.1:n.94dup
NM_003002.4:c.10dup VV MANE Preferred
ENST00000375549.7:c.10dup
ENST00000525291.5:c.10dup
ENST00000525987.5:n.15dup
ENST00000526592.5:c.10dup
ENST00000528021.5:c.10dup
ENST00000528048.5:c.10dup
ENST00000528182.5:c.10dup
ENST00000531744.5:c.10dup
ENST00000532699.1:c.10dup
ENST00000614349.4:c.10dup