Linked Data
dbSNP Id:
rs1690169943
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.202377280A>G , CM000664.2:g.202377280A>G | GRCh38 |
| NC_000002.11:g.203242003A>G , CM000664.1:g.203242003A>G | GRCh37 |
| NC_000002.10:g.202950248A>G | NCBI36 |
| NG_009363.1:g.5954A>G , LRG_712:g.5954A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374580.10:c.-195A>G MANE Select | ENSP00000363708.4:n.-195A>G | |
| ENST00000374580.8:c.-195A>G | ENSP00000363708.4:n.-195A>G | |
| NM_001204.6:c.-195A>G , LRG_712t1:c.-195A>G | NP_001195.2:n.-195A>G | |
| XM_011511687.1:c.-195A>G | XP_011509989.1:n.-195A>G | |
| XM_011511688.1:c.-195A>G | XP_011509990.1:n.-195A>G | |
| NM_001204.7:c.-195A>G MANE Select | NP_001195.2:n.-195A>G |