Linked Data
ClinVar Variation Id:
138455
dbSNP Id:
rs34979001
ExAC:
15:41688700 T / C
gnomAD v2:
15-41688700-T-C
gnomAD v3:
15-41396502-T-C
gnomAD v4:
15-41396502-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.41396502T>C , CM000677.2:g.41396502T>C | GRCh38 |
| NC_000015.9:g.41688700T>C , CM000677.1:g.41688700T>C | GRCh37 |
| NC_000015.8:g.39475992T>C | NCBI36 |
| NG_031924.1:g.10959A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260361.9:c.558A>G MANE Select | ENSP00000260361.4:p.Ile186Met | |
| ENST00000558719.2:c.558A>G | ENSP00000454083.2:p.Ile186Met | |
| ENST00000560978.2:c.558A>G | ENSP00000453944.2:p.Ile186Met | |
| ENST00000676533.1:c.558A>G | ENSP00000504040.1:p.Ile186Met | |
| ENST00000676906.1:c.99A>G | ENSP00000503122.1:p.Ile33Met | |
| ENST00000677477.1:n.1784A>G | ||
| ENST00000678029.1:c.558A>G | ENSP00000503887.1:p.Ile186Met | |
| ENST00000678745.1:c.558A>G | ENSP00000503632.1:p.Ile186Met | |
| ENST00000679094.1:c.558A>G | ENSP00000504295.1:p.Ile186Met | |
| ENST00000679240.1:n.956A>G | ||
| ENST00000260361.8:c.558A>G | ENSP00000260361.4:p.Ile186Met | |
| ENST00000558719.1:c.558A>G | ENSP00000454083.1:p.Ile186Met | |
| ENST00000559127.5:c.558A>G | ENSP00000453027.1:p.Ile186Met | |
| ENST00000560978.1:c.558A>G | ENSP00000453944.1:p.Ile186Met | |
| NM_016013.3:c.558A>G | NP_057097.2:p.Ile186Met | |
| NR_045620.1:n.956A>G | ||
| XM_006720555.1:c.558A>G | XP_006720618.1:p.Ile186Met | |
| XM_011521658.1:c.558A>G | XP_011519960.1:p.Ile186Met | |
| XM_011521659.1:c.558A>G | XP_011519961.1:p.Ile186Met | |
| XM_006720555.3:c.558A>G | XP_006720618.1:p.Ile186Met | |
| XM_011521659.3:c.558A>G | XP_011519961.1:p.Ile186Met | |
| XM_024449945.1:c.558A>G | XP_024305713.1:p.Ile186Met | |
| NM_016013.4:c.558A>G MANE Select | NP_057097.2:p.Ile186Met | |
| NR_045620.2:n.992A>G |