Linked Data
dbSNP Id:
rs1690172056
gnomAD v4:
2-202377377-A-G
MyVariant Identifiers:
chr2:g.203242100A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.202377377A>G , CM000664.2:g.202377377A>G | GRCh38 |
| NC_000002.11:g.203242100A>G , CM000664.1:g.203242100A>G | GRCh37 |
| NC_000002.10:g.202950345A>G | NCBI36 |
| NG_009363.1:g.6051A>G , LRG_712:g.6051A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374580.10:c.-98A>G MANE Select | ENSP00000363708.4:n.-98A>G | |
| ENST00000374580.8:c.-98A>G | ENSP00000363708.4:n.-98A>G | |
| NM_001204.6:c.-98A>G , LRG_712t1:c.-98A>G | NP_001195.2:n.-98A>G | |
| XM_011511687.1:c.-98A>G | XP_011509989.1:n.-98A>G | |
| XM_011511688.1:c.-98A>G | XP_011509990.1:n.-98A>G | |
| NM_001204.7:c.-98A>G MANE Select | NP_001195.2:n.-98A>G |