Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.80276167C= , CM000672.2:g.80276167C= | GRCh38 |
| NC_000010.10:g.82035923C= , CM000672.1:g.82035923C= | GRCh37 |
| NC_000010.9:g.82025903C= | NCBI36 |
| NG_008083.1:g.18512G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000429.3:c.768+209G= MANE Select | NP_000420.1:n.768+209G= |
| ENST00000372213.8:c.768+209G= MANE Select | ENSP00000361287.3:n.768+209G= |
| NM_000429.2:c.768+209G= | NP_000420.1:n.768+209G= |
| ENST00000372213.7:c.768+209G= | ENSP00000361287.3:n.768+209G= |
| XM_005269842.3:c.768+209G= | XP_005269899.1:n.768+209G= |
| XM_005269843.3:c.645+209G= | XP_005269900.1:n.645+209G= |