Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.23509036G= , CM000667.2:g.23509036G= | GRCh38 |
| NC_000005.9:g.23509145G= , CM000667.1:g.23509145G= | GRCh37 |
| NC_000005.8:g.23544902G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502755.6:c.3G= | ENSP00000425471.2:p.Met1= | |
| ENST00000296682.4:c.3G= MANE Select | ENSP00000296682.4:p.Met1= | |
| ENST00000296682.3:c.3G= | ENSP00000296682.3:p.Met1= | |
| ENST00000502755.5:c.3G= | ENSP00000425471.1:p.Met1= | |
| ENST00000635252.1:c.17-884G= | ENSP00000489227.1:n.17-884G= | |
| NM_020227.2:c.3G= | NP_064612.2:p.Met1= | |
| NM_020227.3:c.3G= | NP_064612.2:p.Met1= | |
| NM_001376900.1:c.3G= | NP_001363829.1:p.Met1= | |
| NM_020227.4:c.3G= MANE Select | NP_064612.2:p.Met1= |