Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57139199T= , CM000674.2:g.57139199T= | GRCh38 |
| NC_000012.11:g.57532982T= , CM000674.1:g.57532982T= | GRCh37 |
| NC_000012.10:g.55819249T= | NCBI36 |
| NG_016444.1:g.15701T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002332.3:c.190+618T= MANE Select | NP_002323.2:n.190+618T= |
| ENST00000243077.8:c.190+618T= MANE Select | ENSP00000243077.3:n.190+618T= |
| NM_002332.2:c.190+618T= | NP_002323.2:n.190+618T= |
| ENST00000243077.7:c.190+618T= | ENSP00000243077.3:n.190+618T= |
| ENST00000338962.8:c.190+618T= | ENSP00000341264.4:n.190+618T= |
| ENST00000553277.5:c.190+618T= | ENSP00000451449.1:n.190+618T= |
| ENST00000554174.1:c.190+618T= | ENSP00000451737.1:n.190+618T= |
| XM_017019303.1:c.190+618T= | XP_016874792.1:n.190+618T= |