Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154837602A>T , CM000685.2:g.154837602A>T | GRCh38 |
| NC_000023.10:g.154065877A>T , CM000685.1:g.154065877A>T | GRCh37 |
| NC_000023.9:g.153719071A>T | NCBI36 |
| NG_011403.1:g.190122T>A | |
| NG_033065.1:g.2061T>A | |
| NG_011403.2:g.190122T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000132.4:c.7051T>A MANE Select | NP_000123.1:p.Tyr2351Asn |
| ENST00000360256.9:c.7051T>A MANE Select | ENSP00000353393.4:p.Tyr2351Asn |
| NM_000132.3:c.7051T>A | NP_000123.1:p.Tyr2351Asn |
| NM_019863.2:c.646T>A | NP_063916.1:p.Tyr216Asn |
| NM_019863.3:c.646T>A | NP_063916.1:p.Tyr216Asn |
| ENST00000330287.10:c.646T>A | ENSP00000327895.6:p.Tyr216Asn |
| ENST00000360256.8:c.7051T>A | ENSP00000353393.4:p.Tyr2351Asn |
| ENST00000644698.1:c.784T>A | ENSP00000495706.1:p.Tyr262Asn |
| XM_011531126.1:c.6946T>A | XP_011529428.1:p.Tyr2316Asn |