Linked Data
gnomAD v4:
X-141895122-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.141895122G>T , CM000685.2:g.141895122G>T | GRCh38 |
| NC_000023.10:g.140982908G>T , CM000685.1:g.140982908G>T | GRCh37 |
| NC_000023.9:g.140810574G>T | NCBI36 |
| NG_013272.1:g.61807G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000298296.1:c.910-147G>T MANE Select | ENSP00000298296.1:n.910-147G>T | |
| ENST00000443323.2:c.-118-1309G>T | ENSP00000438254.1:n.-118-1309G>T | |
| ENST00000483584.5:n.150-147G>T | ||
| ENST00000544766.5:c.-378-147G>T | ENSP00000440444.1:n.-378-147G>T | |
| NM_138702.1:c.910-147G>T MANE Select | NP_619647.1:n.910-147G>T | |
| NM_177456.2:c.-378-147G>T | NP_803251.1:n.-378-147G>T | |
| XM_017029265.2:c.-378-147G>T | XP_016884754.1:n.-378-147G>T |