Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.50915501T>C , CM000676.2:g.50915501T>C | GRCh38 |
| NC_000014.8:g.51382219T>C , CM000676.1:g.51382219T>C | GRCh37 |
| NC_000014.7:g.50451969T>C | NCBI36 |
| NG_012796.1:g.34030A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002863.5:c.1240-2A>G MANE Select | NP_002854.3:n.1240-2A>G |
| ENST00000216392.8:c.1240-2A>G MANE Select | ENSP00000216392.7:n.1240-2A>G |
| NM_001163940.1:c.1138-2A>G | NP_001157412.1:n.1138-2A>G |
| NM_001163940.2:c.1138-2A>G | NP_001157412.1:n.1138-2A>G |
| NM_002863.4:c.1240-2A>G | NP_002854.3:n.1240-2A>G |
| ENST00000216392.7:c.1240-2A>G | ENSP00000216392.7:n.1240-2A>G |
| ENST00000528757.2:n.117-2A>G | |
| ENST00000532462.5:c.1240-2A>G | ENSP00000431657.1:n.1240-2A>G |
| ENST00000544180.6:c.1138-2A>G | ENSP00000443787.1:n.1138-2A>G |