Linked Data
gnomAD v4:
14-50944283-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.50944283C>G , CM000676.2:g.50944283C>G | GRCh38 |
| NC_000014.8:g.51411001C>G , CM000676.1:g.51411001C>G | GRCh37 |
| NC_000014.7:g.50480751C>G | NCBI36 |
| NG_012796.1:g.5248G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000216392.8:c.121G>C MANE Select | ENSP00000216392.7:p.Val41Leu | |
| ENST00000216392.7:c.121G>C | ENSP00000216392.7:p.Val41Leu | |
| ENST00000530336.2:n.188G>C | ||
| ENST00000532462.5:c.121G>C | ENSP00000431657.1:p.Val41Leu | |
| ENST00000544180.6:c.121G>C | ENSP00000443787.1:p.Val41Leu | |
| NM_001163940.1:c.121G>C | NP_001157412.1:p.Val41Leu | |
| NM_002863.4:c.121G>C | NP_002854.3:p.Val41Leu | |
| NM_002863.5:c.121G>C MANE Select | NP_002854.3:p.Val41Leu | |
| NM_001163940.2:c.121G>C | NP_001157412.1:p.Val41Leu |