Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154993433T= , CM000685.2:g.154993433T= | GRCh38 |
| NC_000023.10:g.154221708T= , CM000685.1:g.154221708T= | GRCh37 |
| NC_000023.9:g.153874902T= | NCBI36 |
| NG_011403.1:g.34291A= | |
| NG_011403.2:g.34291A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.389-285A= MANE Select | ENSP00000353393.4:n.389-285A= | |
| ENST00000647125.1:c.*175-285A= | ENSP00000496062.1:n.*175-285A= | |
| ENST00000360256.8:c.389-285A= | ENSP00000353393.4:n.389-285A= | |
| ENST00000423959.5:c.284-285A= | ENSP00000409446.1:n.284-285A= | |
| ENST00000453950.1:c.371-285A= | ENSP00000389153.1:n.371-285A= | |
| NM_000132.3:c.389-285A= | NP_000123.1:n.389-285A= | |
| XM_011531126.1:c.284-285A= | XP_011529428.1:n.284-285A= | |
| NM_000132.4:c.389-285A= MANE Select | NP_000123.1:n.389-285A= |