Linked Data
gnomAD v4:
11-67585199-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67585199G>C , CM000673.2:g.67585199G>C | GRCh38 |
| NC_000011.9:g.67352670G>C , CM000673.1:g.67352670G>C | GRCh37 |
| NC_000011.8:g.67109246G>C | NCBI36 |
| NG_012075.1:g.6605G>C , LRG_723:g.6605G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000398603.6:c.294G>C | ENSP00000381604.1:p.Glu98Asp | |
| ENST00000398606.10:c.294G>C MANE Select | ENSP00000381607.3:p.Glu98Asp | |
| ENST00000646888.1:c.*10G>C | ENSP00000494477.1:n.*10G>C | |
| ENST00000398603.5:c.294G>C | ENSP00000381604.1:p.Glu98Asp | |
| ENST00000398606.7:c.294G>C | ENSP00000381607.3:p.Glu98Asp | |
| ENST00000467591.1:n.405G>C | ||
| ENST00000494593.1:n.1089G>C | ||
| ENST00000498765.5:c.357G>C | ||
| NM_000852.3:c.294G>C , LRG_723t1:c.294G>C | NP_000843.1:p.Glu98Asp | |
| NM_000852.4:c.294G>C MANE Select | NP_000843.1:p.Glu98Asp |