Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.4507333G= , CM000671.2:g.4507333G= | GRCh38 |
| NC_000009.11:g.4507333G= , CM000671.1:g.4507333G= | GRCh37 |
| NC_000009.10:g.4497333G= | NCBI36 |
| NG_017044.1:g.21907G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262352.8:c.91+16563G= MANE Select | ENSP00000262352.3:n.91+16563G= | |
| ENST00000262352.7:c.91+16563G= | ENSP00000262352.3:n.91+16563G= | |
| NM_004170.5:c.91+16563G= | NP_004161.4:n.91+16563G= | |
| XM_011518007.1:c.92-12495G= | XP_011516309.1:n.92-12495G= | |
| XM_011518010.1:c.91+16563G= | XP_011516312.1:n.91+16563G= | |
| XM_017015042.1:c.92-12495G= | XP_016870531.1:n.92-12495G= | |
| XM_017015043.1:c.91+16563G= | XP_016870532.1:n.91+16563G= | |
| NM_004170.6:c.91+16563G= MANE Select | NP_004161.4:n.91+16563G= |