Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186079213C>G , CM000666.2:g.186079213C>G | GRCh38 |
| NC_000004.11:g.187000367C>G , CM000666.1:g.187000367C>G | GRCh37 |
| NC_000004.10:g.187237361C>G | NCBI36 |
| NG_007278.1:g.15059C>G , LRG_117:g.15059C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000698351.1:c.633+182C>G | ENSP00000513674.1:n.633+182C>G | |
| ENST00000698352.1:c.*185+182C>G | ENSP00000513675.1:n.*185+182C>G | |
| ENST00000296795.8:c.633+182C>G MANE Select | ENSP00000296795.3:n.633+182C>G | |
| ENST00000296795.7:c.633+182C>G | ENSP00000296795.2:n.633+182C>G | |
| ENST00000513189.1:c.633+182C>G | ENSP00000423386.1:n.633+182C>G | |
| NM_003265.2:c.633+182C>G , LRG_117t1:c.633+182C>G | NP_003256.1:n.633+182C>G | |
| NM_003265.3:c.633+182C>G MANE Select | NP_003256.1:n.633+182C>G |