Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.20993964C>T , CM000684.2:g.20993964C>T | GRCh38 |
| NC_000022.10:g.21348253C>T , CM000684.1:g.21348253C>T | GRCh37 |
| NC_000022.9:g.19678253C>T | NCBI36 |
| NG_034193.1:g.16696C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006767.4:c.1394C>T MANE Select | NP_006758.2:p.Ala465Val |
| ENST00000646124.2:c.1394C>T MANE Select | ENSP00000496779.1:p.Ala465Val |
| NM_006767.3:c.1394C>T | NP_006758.2:p.Ala465Val |
| ENST00000215739.12:c.1394C>T | ENSP00000215739.8:p.Ala465Val |
| ENST00000479606.5:n.1540C>T | |
| ENST00000492480.1:n.443C>T | |
| ENST00000495142.6:n.739C>T | |
| ENST00000642151.1:c.1225C>T | |
| ENST00000643578.1:n.1416C>T | |
| ENST00000643710.1:n.255C>T | |
| ENST00000646506.1:n.973C>T | |
| ENST00000700578.1:c.1394C>T | ENSP00000515073.1:p.Ala465Val |