Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.83075927T>G , CM000667.2:g.83075927T>G | GRCh38 |
| NC_000005.9:g.82371746T>G , CM000667.1:g.82371746T>G | GRCh37 |
| NC_000005.8:g.82407502T>G | NCBI36 |
| NG_047086.1:g.3519T>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_174909.5:c.3+1394A>C MANE Select | NP_777569.1:n.3+1394A>C |
| ENST00000502346.2:c.3+1394A>C MANE Select | ENSP00000424707.1:n.3+1394A>C |
| NM_174909.4:c.3+1394A>C | NP_777569.1:n.3+1394A>C |
| ENST00000502346.1:c.3+1394A>C | ENSP00000424707.1:n.3+1394A>C |
| ENST00000503892.1:n.146+1791A>C | |
| ENST00000504622.5:n.133+1394A>C | |
| ENST00000509770.1:n.104+1394A>C | |
| ENST00000511450.5:n.47+1394A>C |