Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.128300842A= , CM000667.2:g.128300842A= | GRCh38 |
| NC_000005.9:g.127636534A= , CM000667.1:g.127636534A= | GRCh37 |
| NC_000005.8:g.127664433A= | NCBI36 |
| NG_008750.1:g.242202T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000703783.1:n.2925T= | ||
| ENST00000703785.1:n.2844T= | ||
| ENST00000262464.9:c.6141T= MANE Select | ENSP00000262464.4:p.Tyr2047= | |
| ENST00000262464.8:c.6141T= | ENSP00000262464.4:p.Tyr2047= | |
| ENST00000508053.5:c.6141T= | ENSP00000424571.1:p.Tyr2047= | |
| ENST00000619499.4:c.6138T= | ENSP00000482132.1:p.Tyr2046= | |
| NM_001999.3:c.6141T= | NP_001990.2:p.Tyr2047= | |
| XM_017009228.2:c.5988T= | XP_016864717.1:p.Tyr1996= | |
| NM_001999.4:c.6141T= MANE Select | NP_001990.2:p.Tyr2047= |