Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.117676087T>G , CM000668.2:g.117676087T>G | GRCh38 |
| NC_000006.11:g.117997250T>G , CM000668.1:g.117997250T>G | GRCh37 |
| NC_000006.10:g.118103943T>G | NCBI36 |
| NG_054913.1:g.5634T>G | |
| NG_054913.2:g.5634T>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_138459.5:c.415+2T>G MANE Select | NP_612468.1:n.415+2T>G |
| ENST00000368494.4:c.415+2T>G MANE Select | ENSP00000357480.3:n.415+2T>G |
| NM_138459.3:c.415+2T>G | NP_612468.1:n.415+2T>G |
| NM_138459.4:c.415+2T>G | NP_612468.1:n.415+2T>G |
| ENST00000368494.3:c.415+2T>G | ENSP00000357480.3:n.415+2T>G |