Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.135850991G>C , CM000664.2:g.135850991G>C | GRCh38 |
| NC_000002.11:g.136608561G>C , CM000664.1:g.136608561G>C | GRCh37 |
| NC_000002.10:g.136325031G>C | NCBI36 |
| NG_008104.2:g.9179C>G , LRG_338:g.9179C>G | |
| NG_008958.1:g.30451C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000264156.3:c.1917+411C>G MANE Select | ENSP00000264156.2:n.1917+411C>G | |
| ENST00000264156.2:c.1917+411C>G | ENSP00000264156.2:n.1917+411C>G | |
| ENST00000483902.1:n.544+411C>G | ||
| ENST00000492091.1:n.343+411C>G | ||
| NM_005915.5:c.1917+411C>G | NP_005906.2:n.1917+411C>G | |
| NM_005915.6:c.1917+411C>G MANE Select | NP_005906.2:n.1917+411C>G |