Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186676795C= , CM000663.2:g.186676795C= | GRCh38 |
| NC_000001.10:g.186645927C= , CM000663.1:g.186645927C= | GRCh37 |
| NC_000001.9:g.184912550C= | NCBI36 |
| NG_028206.2:g.8633G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000963.4:c.723+38G= MANE Select | NP_000954.1:n.723+38G= |
| ENST00000367468.10:c.723+38G= MANE Select | ENSP00000356438.5:n.723+38G= |
| NM_000963.3:c.723+38G= | NP_000954.1:n.723+38G= |
| ENST00000367468.9:c.723+38G= | ENSP00000356438.5:n.723+38G= |
| ENST00000490885.6:n.856+38G= | |
| ENST00000559627.1:c.613+38G= | ENSP00000454130.1:n.613+38G= |
| ENST00000680451.1:c.723+38G= | ENSP00000506242.1:n.723+38G= |
| ENST00000681605.1:c.*395+38G= | ENSP00000504900.1:n.*395+38G= |