Linked Data
gnomAD v4:
12-5044902-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.5044902T>G , CM000674.2:g.5044902T>G | GRCh38 |
| NC_000012.11:g.5154068T>G , CM000674.1:g.5154068T>G | GRCh37 |
| NC_000012.10:g.5024329T>G | NCBI36 |
| NG_012198.1:g.5984T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252321.5:c.755T>G MANE Select | ENSP00000252321.3:p.Ile252Ser | |
| ENST00000252321.4:c.755T>G | ENSP00000252321.3:p.Ile252Ser | |
| NM_002234.3:c.755T>G | NP_002225.2:p.Ile252Ser | |
| NM_002234.4:c.755T>G MANE Select | NP_002225.2:p.Ile252Ser |