Linked Data
dbSNP Id:
rs2120109468
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.69648083A>T , CM000673.2:g.69648083A>T | GRCh38 |
| NC_000011.9:g.69462851A>T , CM000673.1:g.69462851A>T | GRCh37 |
| NC_000011.8:g.69172032A>T | NCBI36 |
| NG_007375.1:g.11979A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000227507.3:c.664A>T MANE Select | ENSP00000227507.2:p.Asn222Tyr | |
| ENST00000227507.2:c.664A>T | ENSP00000227507.2:p.Asn222Tyr | |
| ENST00000536559.1:c.*84A>T | ENSP00000438482.1:n.*84A>T | |
| ENST00000542367.1:n.127A>T | ||
| ENST00000545484.1:n.370A>T | ||
| NM_053056.2:c.664A>T | NP_444284.1:p.Asn222Tyr | |
| XM_006718653.2:c.688A>T | XP_006718716.1:p.Asn230Tyr | |
| NM_053056.3:c.664A>T MANE Select | NP_444284.1:p.Asn222Tyr |