Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.96287959C= , CM000664.2:g.96287959C= | GRCh38 |
| NC_000002.11:g.96953697C= , CM000664.1:g.96953697C= | GRCh37 |
| NC_000002.10:g.96317424C= | NCBI36 |
| NG_016973.1:g.22601G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_014014.5:c.3269G= MANE Select | NP_054733.2:p.Arg1090= |
| ENST00000323853.10:c.3269G= MANE Select | ENSP00000317123.5:p.Arg1090= |
| NM_014014.4:c.3269G= | NP_054733.2:p.Arg1090= |
| ENST00000323853.9:c.3269G= | ENSP00000317123.5:p.Arg1090= |
| ENST00000480615.1:n.386G= | |
| ENST00000652267.1:c.3269G= | ENSP00000498933.1:p.Arg1090= |