Linked Data
dbSNP Id:
rs1301757809
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.119413871G>C , CM000665.2:g.119413871G>C | GRCh38 |
| NC_000003.11:g.119132718G>C , CM000665.1:g.119132718G>C | GRCh37 |
| NC_000003.10:g.120615408G>C | NCBI36 |
| NG_007665.2:g.124499G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264245.9:c.1942G>C MANE Select | ENSP00000264245.4:p.Ala648Pro | |
| ENST00000264245.8:c.1942G>C | ENSP00000264245.4:p.Ala648Pro | |
| NM_020754.3:c.1942G>C | NP_065805.2:p.Ala648Pro | |
| XM_005247671.3:c.1849G>C | XP_005247728.1:p.Ala617Pro | |
| XM_006713714.2:c.1882G>C | XP_006713777.1:p.Ala628Pro | |
| XM_006713714.3:c.1882G>C | XP_006713777.1:p.Ala628Pro | |
| XM_017006955.1:c.1450G>C | XP_016862444.1:p.Ala484Pro | |
| NM_020754.4:c.1942G>C MANE Select | NP_065805.2:p.Ala648Pro |