Linked Data
gnomAD v4:
16-56983383-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.56983383T>G , CM000678.2:g.56983383T>G | GRCh38 |
| NC_000016.9:g.57017295T>G , CM000678.1:g.57017295T>G | GRCh37 |
| NC_000016.8:g.55574796T>G | NCBI36 |
| NG_008952.1:g.26461T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000200676.8:c.1379T>G MANE Select | ENSP00000200676.3:p.Ile460Ser | |
| ENST00000650358.1:n.1777T>G | ||
| ENST00000200676.7:c.1379T>G | ENSP00000200676.3:p.Ile460Ser | |
| ENST00000379780.6:c.1199T>G | ENSP00000369106.2:p.Ile400Ser | |
| ENST00000566128.1:c.1184T>G | ENSP00000456276.1:p.Ile395Ser | |
| NM_000078.2:c.1379T>G | NP_000069.2:p.Ile460Ser | |
| NM_001286085.1:c.1199T>G | NP_001273014.1:p.Ile400Ser | |
| NM_000078.3:c.1379T>G MANE Select | NP_000069.2:p.Ile460Ser | |
| NM_001286085.2:c.1199T>G | NP_001273014.1:p.Ile400Ser |