Linked Data
gnomAD v4:
5-14871488-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.14871488C>T , CM000667.2:g.14871488C>T | GRCh38 |
| NC_000005.9:g.14871597C>T , CM000667.1:g.14871597C>T | GRCh37 |
| NC_000005.8:g.14924597C>T | NCBI36 |
| NG_008273.1:g.5291G>A | |
| NG_008273.2:g.5298G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000284268.8:c.-41G>A MANE Select | ENSP00000284268.6:n.-41G>A | |
| ENST00000284268.6:c.-41G>A | ENSP00000284268.6:n.-41G>A | |
| ENST00000505140.1:c.-41G>A | ENSP00000426332.1:n.-41G>A | |
| NM_054027.4:c.-41G>A | NP_473368.1:n.-41G>A | |
| XM_011514067.1:c.-41G>A | XP_011512369.1:n.-41G>A | |
| NM_054027.5:c.-41G>A | NP_473368.1:n.-41G>A | |
| NM_054027.6:c.-41G>A MANE Select | NP_473368.1:n.-41G>A |