Linked Data
ClinVar Variation Id:
2927183
ClinVar RCV Id:
RCV003781373
gnomAD v4:
3-128483987-T-C
COSMIC:
COSM4383705
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.128483987T>C , CM000665.2:g.128483987T>C | GRCh38 |
| NC_000003.11:g.128202830T>C , CM000665.1:g.128202830T>C | GRCh37 |
| NC_000003.10:g.129685520T>C | NCBI36 |
| NG_029334.1:g.14201A>G , LRG_295:g.14201A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000487848.6:c.890A>G MANE Plus Clinical | ENSP00000417074.1:p.Asn297Ser | |
| ENST00000696466.1:c.1172A>G | ENSP00000512647.1:p.Asn391Ser | |
| ENST00000341105.7:c.890A>G MANE Select | ENSP00000345681.2:p.Asn297Ser | |
| ENST00000341105.6:c.890A>G | ENSP00000345681.2:p.Asn297Ser | |
| ENST00000430265.6:c.890A>G | ENSP00000400259.2:p.Asn297Ser | |
| ENST00000487848.5:c.890A>G | ENSP00000417074.1:p.Asn297Ser | |
| NM_001145661.1:c.890A>G , LRG_295t1:c.890A>G | NP_001139133.1:p.Asn297Ser | |
| NM_001145662.1:c.890A>G | NP_001139134.1:p.Asn297Ser | |
| NM_032638.4:c.890A>G , LRG_295t2:c.890A>G | NP_116027.2:p.Asn297Ser | |
| NM_001145661.2:c.890A>G MANE Plus Clinical | NP_001139133.1:p.Asn297Ser | |
| NM_032638.5:c.890A>G MANE Select | NP_116027.2:p.Asn297Ser |