Linked Data
ClinVar Variation Id:
444208
dbSNP Id:
rs770983063
ExAC:
1:216595426 T / C
gnomAD v2:
1-216595426-T-C
gnomAD v4:
1-216422084-T-C
COSMIC:
COSM1626818
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.216422084T>C , CM000663.2:g.216422084T>C | GRCh38 |
| NC_000001.10:g.216595426T>C , CM000663.1:g.216595426T>C | GRCh37 |
| NC_000001.9:g.214662049T>C | NCBI36 |
| NG_009497.1:g.6313A>G | |
| NG_009497.2:g.6365A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000307340.8:c.253A>G MANE Select | ENSP00000305941.3:p.Ile85Val | |
| ENST00000674083.1:c.253A>G | ENSP00000501296.1:p.Ile85Val | |
| ENST00000307340.7:c.253A>G | ENSP00000305941.3:p.Ile85Val | |
| ENST00000366942.3:c.253A>G | ENSP00000355909.3:p.Ile85Val | |
| NM_007123.5:c.253A>G | NP_009054.5:p.Ile85Val | |
| NM_206933.2:c.253A>G | NP_996816.2:p.Ile85Val | |
| NM_206933.3:c.253A>G | NP_996816.2:p.Ile85Val | |
| NM_007123.6:c.253A>G | NP_009054.6:p.Ile85Val | |
| NM_206933.4:c.253A>G MANE Select | NP_996816.3:p.Ile85Val |