Canonical Allele Identifier: CA2000559487
Gene: SDHD HGNC NCBI

Linked Data

dbSNP Id: rs1865615217

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112086842del , CM000673.2:g.112086842del GRCh38
NC_000011.9:g.111957566del , CM000673.1:g.111957566del GRCh37
NC_000011.8:g.111462776del NCBI36
NG_012337.2:g.4996del
NG_033145.1:g.4957del
NG_012337.3:g.4996del

Transcript Alleles

HGVS Amino-acid Change
ENST00000640554.1:c.-66del ENSP00000491141.1:n.-66del
ENST00000375549.7:c.-66del ENSP00000364699.3:n.-66del
ENST00000614349.4:c.-66del ENSP00000480666.1:n.-66del
NM_001276503.1:c.-66del NP_001263432.1:n.-66del
NM_001276504.1:c.-66del NP_001263433.1:n.-66del
NM_001276506.1:c.-66del NP_001263435.1:n.-66del
NM_003002.3:c.-66del NP_002993.1:n.-66del
NR_077060.1:n.19del