| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.1090879A= , CM000673.2:g.1090879A= | GRCh38 |
| NC_000011.9:g.1088815A= , CM000673.1:g.1088815A= | GRCh37 |
| NC_000011.8:g.1078815A= | NCBI36 |
| NG_051929.1:g.19518A= |
| HGVS | Amino-acid Change |
|---|---|
| NM_002457.3:c.3600A= | NP_002448.3:p.Ala1200= |
| NM_002457.4:c.3600A= | NP_002448.4:p.Ala1200= |
| ENST00000361558.7:n.3627A= | |
| ENST00000675028.1:c.3600A= | ENSP00000502432.1:p.Ala1200= |