Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.128349443C= , CM000667.2:g.128349443C= | GRCh38 |
| NC_000005.9:g.127685135C= , CM000667.1:g.127685135C= | GRCh37 |
| NC_000005.8:g.127713034C= | NCBI36 |
| NG_008750.1:g.193601G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262464.9:c.2893G= MANE Select | ENSP00000262464.4:p.Val965= | |
| ENST00000262464.8:c.2893G= | ENSP00000262464.4:p.Val965= | |
| ENST00000508053.5:c.2893G= | ENSP00000424571.1:p.Val965= | |
| ENST00000508989.5:c.2794G= | ENSP00000425596.1:p.Val932= | |
| ENST00000619499.4:c.2890G= | ENSP00000482132.1:p.Val964= | |
| NM_001999.3:c.2893G= | NP_001990.2:p.Val965= | |
| XM_017009228.2:c.2740G= | XP_016864717.1:p.Val914= | |
| NM_001999.4:c.2893G= MANE Select | NP_001990.2:p.Val965= |