Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.135798029C= , CM000664.2:g.135798029C= | GRCh38 |
| NC_000002.11:g.136555599C= , CM000664.1:g.136555599C= | GRCh37 |
| NC_000002.10:g.136272069C= | NCBI36 |
| NG_008104.2:g.62141G= , LRG_338:g.62141G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000264162.7:c.4976G= MANE Select | ENSP00000264162.2:p.Arg1659= | |
| ENST00000264162.6:c.4976G= | ENSP00000264162.2:p.Arg1659= | |
| ENST00000452974.1:c.3069G= | ENSP00000391231.1:n.3069G= | |
| NM_002299.2:c.4976G= , LRG_338t1:c.4976G= | NP_002290.2:p.Arg1659= | |
| NM_002299.3:c.4976G= | NP_002290.2:p.Arg1659= | |
| XM_017004088.2:c.4976G= | XP_016859577.1:p.Arg1659= | |
| NM_002299.4:c.4976G= MANE Select | NP_002290.2:p.Arg1659= |