Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.159981673G= , CM000668.2:g.159981673G= | GRCh38 |
| NC_000006.11:g.160402705G= , CM000668.1:g.160402705G= | GRCh37 |
| NC_000006.10:g.160322695G= | NCBI36 |
| NG_011785.3:g.17575G= | |
| NG_011785.4:g.17575G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000876.4:c.150-9511G= MANE Select | NP_000867.3:n.150-9511G= |
| ENST00000356956.6:c.150-9511G= MANE Select | ENSP00000349437.1:n.150-9511G= |
| NM_000876.2:c.150-9511G= | NP_000867.2:n.150-9511G= |
| NM_000876.3:c.150-9511G= | NP_000867.2:n.150-9511G= |
| ENST00000356956.5:c.150-9511G= | ENSP00000349437.1:n.150-9511G= |
| ENST00000676781.1:c.150-9511G= | ENSP00000504419.1:n.150-9511G= |
| ENST00000677704.1:c.150-9511G= | ENSP00000503314.1:n.150-9511G= |
| XR_942419.1:n.165-9511G= |