Linked Data
ClinVar Variation Id:
738189
dbSNP Id:
rs114063013
ExAC:
3:165548755 T / C
gnomAD v2:
3-165548755-T-C
gnomAD v3:
3-165830967-T-C
gnomAD v4:
3-165830967-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.165830967T>C , CM000665.2:g.165830967T>C | GRCh38 |
| NC_000003.11:g.165548755T>C , CM000665.1:g.165548755T>C | GRCh37 |
| NC_000003.10:g.167031449T>C | NCBI36 |
| NG_009031.1:g.11499A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264381.8:c.67A>G MANE Select | ENSP00000264381.3:p.Ile23Val | |
| ENST00000264381.7:c.67A>G | ENSP00000264381.3:p.Ile23Val | |
| ENST00000479451.5:c.107+6347A>G | ENSP00000418325.1:n.107+6347A>G | |
| ENST00000482958.1:c.67A>G | ENSP00000419804.1:p.Ile23Val | |
| ENST00000488954.1:c.107+6347A>G | ENSP00000418504.1:n.107+6347A>G | |
| ENST00000497011.5:c.67A>G | ENSP00000419505.1:p.Ile23Val | |
| NM_000055.2:c.67A>G | NP_000046.1:p.Ile23Val | |
| XM_005247685.1:c.190A>G | XP_005247742.1:p.Ile64Val | |
| NM_000055.3:c.67A>G | NP_000046.1:p.Ile23Val | |
| NR_137635.1:n.159+6347A>G | ||
| NR_137636.1:n.234A>G | ||
| NM_000055.4:c.67A>G MANE Select | NP_000046.1:p.Ile23Val | |
| NR_137635.2:n.110+6347A>G | ||
| NR_137636.2:n.185A>G |