Linked Data
gnomAD v4:
X-153690460-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153690460G>T , CM000685.2:g.153690460G>T | GRCh38 |
| NC_000023.10:g.152955915G>T , CM000685.1:g.152955915G>T | GRCh37 |
| NC_000023.9:g.152609109G>T | NCBI36 |
| NG_012016.1:g.7164G>T | |
| NG_012016.2:g.7164G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000253122.10:c.348G>T MANE Select | ENSP00000253122.5:p.Met116Ile | |
| ENST00000675713.1:n.102G>T | ||
| ENST00000253122.9:c.348G>T | ENSP00000253122.5:p.Met116Ile | |
| ENST00000430077.6:c.3G>T | ENSP00000403041.2:p.Met1Ile | |
| ENST00000476466.1:n.200G>T | ||
| NM_001142805.1:c.348G>T | NP_001136277.1:p.Met116Ile | |
| NM_001142806.1:c.3G>T | NP_001136278.1:p.Met1Ile | |
| NM_005629.3:c.348G>T | NP_005620.1:p.Met116Ile | |
| NM_005629.4:c.348G>T MANE Select | NP_005620.1:p.Met116Ile | |
| NM_001142805.2:c.348G>T | NP_001136277.1:p.Met116Ile |