Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.49636587A= , CM000681.2:g.49636587A= | GRCh38 |
| NC_000019.9:g.50139844A= , CM000681.1:g.50139844A= | GRCh37 |
| NC_000019.8:g.54831656A= | NCBI36 |
| NG_042222.1:g.8557T= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000246792.4:c.453+32T= MANE Select | ENSP00000246792.2:n.453+32T= | |
| ENST00000246792.3:c.453+32T= | ENSP00000246792.2:n.453+32T= | |
| ENST00000601532.1:n.593+32T= | ||
| NM_006270.3:c.453+32T= | NP_006261.1:n.453+32T= | |
| NM_006270.4:c.453+32T= | NP_006261.1:n.453+32T= | |
| NM_006270.5:c.453+32T= MANE Select | NP_006261.1:n.453+32T= |