Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.67940365C= , CM000678.2:g.67940365C= | GRCh38 |
| NC_000016.9:g.67974268C= , CM000678.1:g.67974268C= | GRCh37 |
| NC_000016.8:g.66531769C= | NCBI36 |
| NG_009778.1:g.8748G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264005.10:c.862G= MANE Select | ENSP00000264005.5:p.Val288= | |
| ENST00000264005.9:c.862G= | ENSP00000264005.5:p.Val288= | |
| ENST00000570369.5:c.156-291G= | ||
| ENST00000570980.1:c.646G= | ENSP00000464651.1:p.Val216= | |
| ENST00000573538.5:c.600G= | ENSP00000463220.1:n.600G= | |
| NM_000229.1:c.862G= | NP_000220.1:p.Val288= | |
| NM_000229.2:c.862G= MANE Select | NP_000220.1:p.Val288= |