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