Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.115731017A>G , CM000663.2:g.115731017A>G | GRCh38 |
| NC_000001.10:g.116273638A>G , CM000663.1:g.116273638A>G | GRCh37 |
| NC_000001.9:g.116075161A>G | NCBI36 |
| NG_008802.1:g.42789T>C , LRG_404:g.42789T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000488931.2:c.425+1097T>C | ENSP00000518226.1:n.425+1097T>C | |
| ENST00000261448.6:c.606+1884T>C MANE Select | ENSP00000261448.5:n.606+1884T>C | |
| ENST00000261448.5:c.606+1884T>C | ENSP00000261448.5:n.606+1884T>C | |
| ENST00000488931.1:n.122+1097T>C | ||
| NM_001232.3:c.606+1884T>C , LRG_404t1:c.606+1884T>C | NP_001223.2:n.606+1884T>C | |
| NM_001232.4:c.606+1884T>C MANE Select | NP_001223.2:n.606+1884T>C |