Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.128357125C= , CM000667.2:g.128357125C= | GRCh38 |
| NC_000005.9:g.127692817C= , CM000667.1:g.127692817C= | GRCh37 |
| NC_000005.8:g.127720716C= | NCBI36 |
| NG_008750.1:g.185919G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262464.9:c.2674+151G= MANE Select | ENSP00000262464.4:n.2674+151G= | |
| ENST00000262464.8:c.2674+151G= | ENSP00000262464.4:n.2674+151G= | |
| ENST00000508053.5:c.2674+151G= | ENSP00000424571.1:n.2674+151G= | |
| ENST00000508989.5:c.2575+151G= | ENSP00000425596.1:n.2575+151G= | |
| ENST00000619499.4:c.2671+151G= | ENSP00000482132.1:n.2671+151G= | |
| NM_001999.3:c.2674+151G= | NP_001990.2:n.2674+151G= | |
| XM_017009228.2:c.2521+151G= | XP_016864717.1:n.2521+151G= | |
| NM_001999.4:c.2674+151G= MANE Select | NP_001990.2:n.2674+151G= |