Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.86344769C= , CM000672.2:g.86344769C= | GRCh38 |
| NC_000010.10:g.88104526C= , CM000672.1:g.88104526C= | GRCh37 |
| NC_000010.9:g.88094506C= | NCBI36 |
| NG_011875.1:g.26725G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_017551.3:c.235+19172G= MANE Select | NP_060021.1:n.235+19172G= |
| ENST00000327946.12:c.235+19172G= MANE Select | ENSP00000330148.7:n.235+19172G= |
| NM_017551.2:c.235+19172G= | NP_060021.1:n.235+19172G= |
| ENST00000327946.11:c.235+19172G= | ENSP00000330148.7:n.235+19172G= |
| ENST00000464741.2:c.235+19172G= | ENSP00000433064.1:n.235+19172G= |
| XM_011539720.1:c.235+19172G= | XP_011538022.1:n.235+19172G= |
| XM_011539720.2:c.235+19172G= | XP_011538022.1:n.235+19172G= |