Linked Data
dbSNP Id:
rs1251666247
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.112086798del , CM000673.2:g.112086798del | GRCh38 |
| NC_000011.9:g.111957522del , CM000673.1:g.111957522del | GRCh37 |
| NC_000011.8:g.111462732del | NCBI36 |
| NG_012337.2:g.4952del | |
| NG_033145.1:g.5002del | |
| NG_012337.3:g.4952del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375549.7:c.-110del (SDHD) | ENSP00000364699.3:n.-110del | |
| ENST00000509359.6:c.-74del (TIMM8B) | ENSP00000421964.2:n.-74del | |
| ENST00000541231.1:c.-29del (TIMM8B) | ENSP00000438455.1:n.-29del | |
| NM_012459.2:c.-29del (TIMM8B) | NP_036591.2:n.-29del | |
| NR_028383.1:n.2del (TIMM8B) |