Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186079210G>C , CM000666.2:g.186079210G>C | GRCh38 |
| NC_000004.11:g.187000364G>C , CM000666.1:g.187000364G>C | GRCh37 |
| NC_000004.10:g.187237358G>C | NCBI36 |
| NG_007278.1:g.15056G>C , LRG_117:g.15056G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_003265.3:c.633+179G>C MANE Select | NP_003256.1:n.633+179G>C |
| ENST00000296795.8:c.633+179G>C MANE Select | ENSP00000296795.3:n.633+179G>C |
| NM_003265.2:c.633+179G>C , LRG_117t1:c.633+179G>C | NP_003256.1:n.633+179G>C |
| ENST00000296795.7:c.633+179G>C | ENSP00000296795.2:n.633+179G>C |
| ENST00000513189.1:c.633+179G>C | ENSP00000423386.1:n.633+179G>C |
| ENST00000698351.1:c.633+179G>C | ENSP00000513674.1:n.633+179G>C |
| ENST00000698352.1:c.*185+179G>C | ENSP00000513675.1:n.*185+179G>C |