Linked Data
dbSNP Id:
rs2038918383
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.74920046G>A , CM000679.2:g.74920046G>A | GRCh38 |
| NC_000017.10:g.72916141G>A , CM000679.1:g.72916141G>A | GRCh37 |
| NC_000017.9:g.70427736G>A | NCBI36 |
| NG_007882.1:g.8211C>T | |
| NG_033062.1:g.772G>A | |
| NG_007882.2:g.8218C>T | |
| NG_033062.2:g.772G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000614341.5:c.790C>T MANE Select | ENSP00000480279.1:p.Pro264Ser | |
| ENST00000579243.1:c.*389C>T | ENSP00000462568.1:n.*389C>T | |
| ENST00000614341.4:c.790C>T | ENSP00000480279.1:p.Pro264Ser | |
| NM_001282489.2:c.481C>T | NP_001269418.1:p.Pro161Ser | |
| NM_173477.4:c.790C>T | NP_775748.2:p.Pro264Ser | |
| XM_011524296.1:c.481C>T | XP_011522598.1:p.Pro161Ser | |
| XM_011524296.2:c.481C>T | XP_011522598.1:p.Pro161Ser | |
| NM_173477.5:c.790C>T MANE Select | NP_775748.2:p.Pro264Ser | |
| NM_001282489.3:c.481C>T | NP_001269418.1:p.Pro161Ser |