Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.17022531A= , CM000663.2:g.17022531A= | GRCh38 |
| NC_000001.10:g.17349026A= , CM000663.1:g.17349026A= | GRCh37 |
| NC_000001.9:g.17221613A= | NCBI36 |
| NG_012340.1:g.36640T= , LRG_316:g.36640T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000463045.3:c.594+77T= | ENSP00000481376.2:n.594+77T= | |
| ENST00000491274.6:c.723+77T= | ENSP00000480482.2:n.723+77T= | |
| ENST00000375499.8:c.765+77T= MANE Select | ENSP00000364649.3:n.765+77T= | |
| ENST00000375499.7:c.765+77T= | ENSP00000364649.3:n.765+77T= | |
| ENST00000475049.5:n.190+77T= | ||
| ENST00000485092.5:n.429+77T= | ||
| NM_003000.2:c.765+77T= , LRG_316t1:c.765+77T= | NP_002991.2:n.765+77T= | |
| NM_003000.3:c.765+77T= MANE Select | NP_002991.2:n.765+77T= |