Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.232539987T= , CM000664.2:g.232539987T= | GRCh38 |
| NC_000002.11:g.233404697T= , CM000664.1:g.233404697T= | GRCh37 |
| NC_000002.10:g.233112941T= | NCBI36 |
| NG_012954.1:g.5261T= | |
| NG_012954.2:g.5296T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000651502.1:c.56-5T= MANE Select | ENSP00000498757.1:n.56-5T= | |
| ENST00000389492.3:c.56-5T= | ENSP00000374143.3:n.56-5T= | |
| ENST00000389494.7:c.56-5T= | ENSP00000374145.3:n.56-5T= | |
| ENST00000485094.1:n.77-5T= | ||
| NM_005199.4:c.56-5T= | NP_005190.4:n.56-5T= | |
| NM_005199.5:c.56-5T= MANE Select | NP_005190.4:n.56-5T= |