Linked Data
MyVariant Identifiers:
chr3:g.190126170T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.190408381T>G , CM000665.2:g.190408381T>G | GRCh38 |
| NC_000003.11:g.190126170T>G , CM000665.1:g.190126170T>G | GRCh37 |
| NC_000003.10:g.191608864T>G | NCBI36 |
| NG_008149.1:g.25330T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264734.3:c.450T>G MANE Select | ENSP00000264734.3:p.Val150= | |
| ENST00000456423.2:c.115-1522T>G | ENSP00000414136.2:n.115-1522T>G | |
| ENST00000264734.2:c.660T>G | ENSP00000264734.2:p.Val220= | |
| ENST00000456423.1:c.325-1522T>G | ENSP00000414136.1:n.325-1522T>G | |
| NM_006580.3:c.660T>G | NP_006571.1:p.Val220= | |
| NM_001378492.1:c.450T>G | NP_001365421.1:p.Val150= | |
| NM_001378493.1:c.450T>G | NP_001365422.1:p.Val150= | |
| NM_006580.4:c.450T>G MANE Select | NP_006571.2:p.Val150= |