Linked Data
dbSNP Id:
rs2084174606
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.45293301C>T , CM000684.2:g.45293301C>T | GRCh38 |
| NC_000022.10:g.45689182C>T , CM000684.1:g.45689182C>T | GRCh37 |
| NC_000022.9:g.44067846C>T | NCBI36 |
| NG_016203.1:g.13315C>T | |
| NG_016203.2:g.13315C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000216211.9:c.692C>T MANE Select | ENSP00000216211.4:p.Ala231Val | |
| ENST00000216211.8:c.692C>T | ENSP00000216211.4:p.Ala231Val | |
| ENST00000396082.2:c.329C>T | ENSP00000379391.2:p.Ala110Val | |
| NM_001167574.1:c.329C>T | NP_001161046.1:p.Ala110Val | |
| NM_006953.3:c.692C>T | NP_008884.1:p.Ala231Val | |
| XM_011530364.1:c.698C>T | XP_011528666.1:p.Ala233Val | |
| XM_011530365.1:c.335C>T | XP_011528667.1:p.Ala112Val | |
| NM_006953.4:c.692C>T MANE Select | NP_008884.1:p.Ala231Val | |
| NM_001167574.2:c.329C>T | NP_001161046.1:p.Ala110Val |