Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.50905414G>T , CM000676.2:g.50905414G>T | GRCh38 |
| NC_000014.8:g.51372132G>T , CM000676.1:g.51372132G>T | GRCh37 |
| NC_000014.7:g.50441882G>T | NCBI36 |
| NG_012796.1:g.44117C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000216392.8:c.2522C>A MANE Select | ENSP00000216392.7:p.Ser841Tyr | |
| ENST00000216392.7:c.2522C>A | ENSP00000216392.7:p.Ser841Tyr | |
| ENST00000532462.5:c.2379+2857C>A | ENSP00000431657.1:n.2379+2857C>A | |
| ENST00000544180.6:c.2420C>A | ENSP00000443787.1:p.Ser807Tyr | |
| NM_001163940.1:c.2420C>A | NP_001157412.1:p.Ser807Tyr | |
| NM_002863.4:c.2522C>A | NP_002854.3:p.Ser841Tyr | |
| NM_002863.5:c.2522C>A MANE Select | NP_002854.3:p.Ser841Tyr | |
| NM_001163940.2:c.2420C>A | NP_001157412.1:p.Ser807Tyr |