Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.147830496T>C , CM000667.2:g.147830496T>C | GRCh38 |
| NC_000005.9:g.147210059T>C , CM000667.1:g.147210059T>C | GRCh37 |
| NC_000005.8:g.147190252T>C | NCBI36 |
| NG_008356.2:g.13736A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296695.10:c.56-866A>G MANE Select | ENSP00000296695.5:n.56-866A>G | |
| ENST00000296695.9:c.56-866A>G | ENSP00000296695.5:n.56-866A>G | |
| ENST00000510027.2:c.56-866A>G | ENSP00000427376.1:n.56-866A>G | |
| NM_003122.4:c.56-866A>G | NP_003113.2:n.56-866A>G | |
| NM_001354966.1:c.56-866A>G | NP_001341895.1:n.56-866A>G | |
| NM_001354966.2:c.56-866A>G | NP_001341895.1:n.56-866A>G | |
| NM_001379610.1:c.56-866A>G MANE Select | NP_001366539.1:n.56-866A>G | |
| NM_003122.5:c.56-866A>G | NP_003113.2:n.56-866A>G |