Linked Data
dbSNP Id:
rs901836262
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.50910088C>T , CM000676.2:g.50910088C>T | GRCh38 |
| NC_000014.8:g.51376806C>T , CM000676.1:g.51376806C>T | GRCh37 |
| NC_000014.7:g.50446556C>T | NCBI36 |
| NG_012796.1:g.39443G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000216392.8:c.1984G>A MANE Select | ENSP00000216392.7:p.Asp662Asn | |
| ENST00000216392.7:c.1984G>A | ENSP00000216392.7:p.Asp662Asn | |
| ENST00000532107.2:n.157G>A | ||
| ENST00000532462.5:c.1984G>A | ENSP00000431657.1:p.Asp662Asn | |
| ENST00000544180.6:c.1882G>A | ENSP00000443787.1:p.Asp628Asn | |
| NM_001163940.1:c.1882G>A | NP_001157412.1:p.Asp628Asn | |
| NM_002863.4:c.1984G>A | NP_002854.3:p.Asp662Asn | |
| NM_002863.5:c.1984G>A MANE Select | NP_002854.3:p.Asp662Asn | |
| NM_001163940.2:c.1882G>A | NP_001157412.1:p.Asp628Asn |