Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.149978091G= , CM000667.2:g.149978091G= | GRCh38 |
| NC_000005.9:g.149357654G= , CM000667.1:g.149357654G= | GRCh37 |
| NC_000005.8:g.149337847G= | NCBI36 |
| NG_007147.2:g.19209G= , LRG_684:g.19209G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000690410.1:n.671G= | ||
| ENST00000286298.5:c.439G= MANE Select | ENSP00000286298.4:p.Ala147= | |
| ENST00000286298.4:c.439G= | ENSP00000286298.4:p.Ala147= | |
| ENST00000503336.1:c.112G= | ENSP00000426053.1:p.Ala38= | |
| NM_000112.3:c.439G= , LRG_684t1:c.439G= | NP_000103.2:p.Ala147= | |
| XM_017009191.2:c.439G= | XP_016864680.1:p.Ala147= | |
| NM_000112.4:c.439G= MANE Select | NP_000103.2:p.Ala147= |