Linked Data
dbSNP Id:
rs1762738261
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32443385C>A , CM000668.2:g.32443385C>A | GRCh38 |
| NC_000006.11:g.32411162C>A , CM000668.1:g.32411162C>A | GRCh37 |
| NC_000006.10:g.32519140C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000395388.7:c.529C>A MANE Select | ENSP00000378786.2:p.Pro177Thr | |
| ENST00000374982.5:c.454C>A | ENSP00000364121.5:p.Pro152Thr | |
| ENST00000395388.6:c.529C>A | ENSP00000378786.2:p.Pro177Thr | |
| NM_019111.4:c.529C>A | NP_061984.2:p.Pro177Thr | |
| NM_019111.5:c.529C>A MANE Select | NP_061984.2:p.Pro177Thr |