MyVariant.info:
GRCh37
chr3:g.186338425A>G
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.186620636A>G , CM000665.2:g.186620636A>G | GRCh38 |
| NC_000003.11:g.186338425A>G , CM000665.1:g.186338425A>G | GRCh37 |
| NC_000003.10:g.187821119A>G | NCBI36 |
| NG_011436.1:g.12576A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000411641.7:c.810A>G MANE Select | ENSP00000393887.2:p.Thr270= | |
| ENST00000273784.5:c.813A>G | ENSP00000273784.5:p.Thr271= | |
| ENST00000411641.6:c.810A>G | ENSP00000393887.2:p.Thr270= | |
| NM_001622.2:c.810A>G | NP_001613.2:p.Thr270= | |
| NM_001354571.1:c.813A>G | NP_001341500.1:p.Thr271= | |
| NM_001354572.1:c.807A>G | NP_001341501.1:p.Thr269= | |
| NM_001354573.1:c.726A>G | NP_001341502.1:p.Thr242= | |
| NM_001622.3:c.810A>G | NP_001613.2:p.Thr270= | |
| NM_001622.4:c.810A>G MANE Select | NP_001613.2:p.Thr270= | |
| NM_001354571.2:c.813A>G | NP_001341500.1:p.Thr271= | |
| NM_001354572.2:c.807A>G | NP_001341501.1:p.Thr269= | |
| NM_001354573.2:c.726A>G | NP_001341502.1:p.Thr242= |