Linked Data
gnomAD v4:
13-110179243-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.110179243C>T , CM000675.2:g.110179243C>T | GRCh38 |
| NC_000013.10:g.110831590C>T , CM000675.1:g.110831590C>T | GRCh37 |
| NC_000013.9:g.109629591C>T | NCBI36 |
| NG_011544.2:g.132907G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375820.10:c.2344+28G>A MANE Select | ENSP00000364979.4:n.2344+28G>A | |
| ENST00000649738.1:n.2474+28G>A | ||
| ENST00000375820.8:c.2344+28G>A | ENSP00000364979.4:n.2344+28G>A | |
| NM_001845.5:c.2344+28G>A | NP_001836.3:n.2344+28G>A | |
| XM_011521048.1:c.2152+28G>A | XP_011519350.1:n.2152+28G>A | |
| XM_011521048.2:c.2152+28G>A | XP_011519350.1:n.2152+28G>A | |
| NM_001845.6:c.2344+28G>A MANE Select | NP_001836.3:n.2344+28G>A |