Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.17022187A= , CM000663.2:g.17022187A= | GRCh38 |
| NC_000001.10:g.17348682A= , CM000663.1:g.17348682A= | GRCh37 |
| NC_000001.9:g.17221269A= | NCBI36 |
| NG_012340.1:g.36984T= , LRG_316:g.36984T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000463045.3:c.594+421T= | ENSP00000481376.2:n.594+421T= | |
| ENST00000491274.6:c.723+421T= | ENSP00000480482.2:n.723+421T= | |
| ENST00000375499.8:c.765+421T= MANE Select | ENSP00000364649.3:n.765+421T= | |
| ENST00000375499.7:c.765+421T= | ENSP00000364649.3:n.765+421T= | |
| ENST00000475049.5:n.190+421T= | ||
| ENST00000485092.5:n.429+421T= | ||
| NM_003000.2:c.765+421T= , LRG_316t1:c.765+421T= | NP_002991.2:n.765+421T= | |
| NM_003000.3:c.765+421T= MANE Select | NP_002991.2:n.765+421T= |