Linked Data
dbSNP Id:
rs1681788109
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.18143693T>A , CM000668.2:g.18143693T>A | GRCh38 |
| NC_000006.11:g.18143924T>A , CM000668.1:g.18143924T>A | GRCh37 |
| NC_000006.10:g.18251903T>A | NCBI36 |
| NG_012137.2:g.16451A>T | |
| NG_012137.3:g.16451A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000309983.5:c.269A>T MANE Select | ENSP00000312304.4:p.Glu90Val | |
| ENST00000309983.4:c.269A>T | ENSP00000312304.4:p.Glu90Val | |
| NM_000367.3:c.269A>T | NP_000358.1:p.Glu90Val | |
| XM_011514839.1:c.269A>T | XP_011513141.1:p.Glu90Val | |
| XM_011514840.1:c.200A>T | XP_011513142.1:p.Glu67Val | |
| NM_000367.4:c.269A>T | NP_000358.1:p.Glu90Val | |
| NM_001346817.1:c.269A>T | NP_001333746.1:p.Glu90Val | |
| NM_001346818.1:c.269A>T | NP_001333747.1:p.Glu90Val | |
| NM_000367.5:c.269A>T MANE Select | NP_000358.1:p.Glu90Val |