Linked Data
gnomAD v4:
14-91272503-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.91272503G>T , CM000676.2:g.91272503G>T | GRCh38 |
| NC_000014.8:g.91738847G>T , CM000676.1:g.91738847G>T | GRCh37 |
| NC_000014.7:g.90808600G>T | NCBI36 |
| NG_033118.1:g.150342C>A | |
| NG_033118.2:g.150342C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000389857.11:c.*122C>A MANE Select | ENSP00000374507.6:n.*122C>A | |
| ENST00000331194.8:c.*122C>A | ENSP00000330332.8:n.*122C>A | |
| ENST00000389857.10:c.*122C>A | ENSP00000374507.6:n.*122C>A | |
| ENST00000556726.5:c.2437C>A | ||
| NM_001080414.3:c.*122C>A | NP_001073883.2:n.*122C>A | |
| XM_011536796.1:c.*122C>A | XP_011535098.1:n.*122C>A | |
| XM_011536796.2:c.*122C>A | XP_011535098.1:n.*122C>A | |
| XM_017021336.1:c.*122C>A | XP_016876825.1:n.*122C>A | |
| NM_001080414.4:c.*122C>A MANE Select | NP_001073883.2:n.*122C>A |