Linked Data
ClinVar Variation Id:
1479143
ClinVar RCV Id:
RCV001976636
dbSNP Id:
rs771264308
ExAC:
2:25965191 T / C
gnomAD v2:
2-25965191-T-C
gnomAD v3:
2-25742322-T-C
gnomAD v4:
2-25742322-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.25742322T>C , CM000664.2:g.25742322T>C | GRCh38 |
| NC_000002.11:g.25965191T>C , CM000664.1:g.25965191T>C | GRCh37 |
| NC_000002.10:g.25818695T>C | NCBI36 |
| NG_052995.1:g.141195A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000336112.9:c.4012A>G | ENSP00000337250.5:p.Met1338Val | |
| ENST00000435504.9:c.4015A>G MANE Select | ENSP00000391447.3:p.Met1339Val | |
| ENST00000336112.8:c.3931A>G | ENSP00000337250.4:p.Met1311Val | |
| ENST00000404843.5:c.2464A>G | ENSP00000383920.1:p.Met822Val | |
| ENST00000435504.8:c.4015A>G | ENSP00000391447.3:p.Met1339Val | |
| NM_018263.4:c.4015A>G | NP_060733.4:p.Met1339Val | |
| XM_006712039.2:c.3649A>G | XP_006712102.1:p.Met1217Val | |
| XM_006712040.1:c.3235A>G | XP_006712103.1:p.Met1079Val | |
| XM_011532950.1:c.4012A>G | XP_011531252.1:p.Met1338Val | |
| XM_011532951.1:c.3841A>G | XP_011531253.1:p.Met1281Val | |
| NM_018263.5:c.4015A>G | NP_060733.4:p.Met1339Val | |
| XM_006712039.3:c.3649A>G | XP_006712102.1:p.Met1217Val | |
| XM_006712040.2:c.3235A>G | XP_006712103.1:p.Met1079Val | |
| XM_011532950.3:c.4012A>G | XP_011531252.1:p.Met1338Val | |
| XM_011532951.2:c.3841A>G | XP_011531253.1:p.Met1281Val | |
| XM_017004430.1:c.3235A>G | XP_016859919.1:p.Met1079Val | |
| XM_024452974.1:c.4195A>G | XP_024308742.1:p.Met1399Val | |
| NM_001369346.1:c.3841A>G | NP_001356275.1:p.Met1281Val | |
| NM_001369347.1:c.3235A>G | NP_001356276.1:p.Met1079Val | |
| NM_018263.6:c.4015A>G MANE Select | NP_060733.4:p.Met1339Val |