Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.135807131A= , CM000664.2:g.135807131A= | GRCh38 |
| NC_000002.11:g.136564701A= , CM000664.1:g.136564701A= | GRCh37 |
| NC_000002.10:g.136281171A= | NCBI36 |
| NG_008104.2:g.53039T= , LRG_338:g.53039T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002299.4:c.4170T= MANE Select | NP_002290.2:p.Tyr1390= |
| ENST00000264162.7:c.4170T= MANE Select | ENSP00000264162.2:p.Tyr1390= |
| NM_002299.2:c.4170T= , LRG_338t1:c.4170T= | NP_002290.2:p.Tyr1390= |
| NM_002299.3:c.4170T= | NP_002290.2:p.Tyr1390= |
| ENST00000264162.6:c.4170T= | ENSP00000264162.2:p.Tyr1390= |
| ENST00000452974.1:c.2466T= | ENSP00000391231.1:p.Tyr822= |
| XM_017004088.2:c.4170T= | XP_016859577.1:p.Tyr1390= |