Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.46085716A>C , CM000666.2:g.46085716A>C | GRCh38 |
| NC_000004.11:g.46087733A>C , CM000666.1:g.46087733A>C | GRCh37 |
| NC_000004.10:g.45782490A>C | NCBI36 |
| NG_046964.1:g.43350T>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_173536.4:c.254-1663T>G MANE Select | NP_775807.2:n.254-1663T>G |
| ENST00000295452.5:c.254-1663T>G MANE Select | ENSP00000295452.4:n.254-1663T>G |
| NM_173536.3:c.254-1663T>G | NP_775807.2:n.254-1663T>G |
| ENST00000295452.4:c.254-1663T>G | ENSP00000295452.4:n.254-1663T>G |