Linked Data
ClinVar Variation Id:
2143661
ClinVar RCV Id:
RCV003062770
dbSNP Id:
rs782377148
ExAC:
11:118896742 T / C
gnomAD v2:
11-118896742-T-C
gnomAD v4:
11-119026032-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.119026032T>C , CM000673.2:g.119026032T>C | GRCh38 |
| NC_000011.9:g.118896742T>C , CM000673.1:g.118896742T>C | GRCh37 |
| NC_000011.8:g.118401952T>C | NCBI36 |
| NG_013331.1:g.9874A>G , LRG_187:g.9874A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000529510.6:n.1063A>G | ||
| ENST00000697845.1:n.1843A>G | ||
| ENST00000697846.1:n.1063A>G | ||
| ENST00000697847.1:n.1202-275A>G | ||
| ENST00000697848.1:n.1149A>G | ||
| ENST00000697849.1:n.2958A>G | ||
| ENST00000697850.1:n.1149A>G | ||
| ENST00000697851.1:n.2757A>G | ||
| ENST00000638186.1:n.1223A>G | ||
| ENST00000638360.1:n.1055A>G | ||
| ENST00000638925.1:n.1188A>G | ||
| ENST00000650539.1:n.1325A>G | ||
| ENST00000330775.9:c.919A>G | ENSP00000476242.2:p.Met307Val | |
| ENST00000357590.9:c.919A>G | ENSP00000476176.2:p.Met307Val | |
| ENST00000524428.5:n.1155A>G | ||
| ENST00000525039.5:n.1343A>G | ||
| ENST00000525102.5:n.1677A>G | ||
| ENST00000525372.5:n.1017A>G | ||
| ENST00000526275.5:n.1701A>G | ||
| ENST00000527992.5:n.1147A>G | ||
| ENST00000529510.5:n.607A>G | ||
| ENST00000530407.5:n.1069A>G | ||
| ENST00000532085.1:n.4300A>G | ||
| ENST00000538950.5:c.700A>G | ENSP00000475991.2:p.Met234Val | |
| ENST00000545985.5:c.919A>G | ENSP00000475241.2:p.Met307Val | |
| NM_001164277.1:c.919A>G , LRG_187t1:c.919A>G | NP_001157749.1:p.Met307Val | |
| NM_001164278.1:c.919A>G | NP_001157750.1:p.Met307Val | |
| NM_001164279.1:c.700A>G | NP_001157751.1:p.Met234Val | |
| NM_001164280.1:c.919A>G | NP_001157752.1:p.Met307Val | |
| NM_001467.5:c.919A>G | NP_001458.1:p.Met307Val | |
| NM_001164278.2:c.919A>G | NP_001157750.1:p.Met307Val | |
| NM_001164279.2:c.700A>G | NP_001157751.1:p.Met234Val | |
| NM_001164280.2:c.919A>G | NP_001157752.1:p.Met307Val | |
| NM_001467.6:c.919A>G | NP_001458.1:p.Met307Val | |
| NM_001164277.2:c.919A>G MANE Select | NP_001157749.1:p.Met307Val |