Linked Data
gnomAD v4:
10-104057169-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.104057169A>C , CM000672.2:g.104057169A>C | GRCh38 |
| NC_000010.10:g.105816927A>C , CM000672.1:g.105816927A>C | GRCh37 |
| NC_000010.9:g.105806917A>C | NCBI36 |
| NG_007069.1:g.33712T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000369733.8:c.1271T>G | ENSP00000358748.3:p.Ile424Ser | |
| ENST00000648076.2:c.1271T>G MANE Select | ENSP00000497653.1:p.Ile424Ser | |
| ENST00000650263.1:c.1223T>G | ENSP00000497850.1:p.Ile408Ser | |
| ENST00000353479.9:c.1271T>G | ENSP00000340937.5:p.Ile424Ser | |
| ENST00000369733.7:c.1271T>G | ENSP00000358748.3:p.Ile424Ser | |
| NM_000494.3:c.1271T>G | NP_000485.3:p.Ile424Ser | |
| NM_000494.4:c.1271T>G MANE Select | NP_000485.3:p.Ile424Ser |