Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.190388331T= , CM000665.2:g.190388331T= | GRCh38 |
| NC_000003.11:g.190106120T= , CM000665.1:g.190106120T= | GRCh37 |
| NC_000003.10:g.191588814T= | NCBI36 |
| NG_008149.1:g.5280T= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000264734.3:c.2T= MANE Select | ENSP00000264734.3:p.Met1= | |
| ENST00000456423.2:c.2T= | ENSP00000414136.2:p.Met1= | |
| ENST00000264734.2:c.212T= | ENSP00000264734.2:p.Met71= | |
| ENST00000456423.1:c.212T= | ENSP00000414136.1:p.Met71= | |
| ENST00000468220.1:n.306+13728T= | ||
| NM_006580.3:c.212T= | NP_006571.1:p.Met71= | |
| NM_001378492.1:c.2T= | NP_001365421.1:p.Met1= | |
| NM_001378493.1:c.2T= | NP_001365422.1:p.Met1= | |
| NM_006580.4:c.2T= MANE Select | NP_006571.2:p.Met1= |