Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.35284909C>G , CM000681.2:g.35284909C>G | GRCh38 |
| NC_000019.9:g.35775812C>G , CM000681.1:g.35775812C>G | GRCh37 |
| NC_000019.8:g.40467652C>G | NCBI36 |
| NG_011563.1:g.7403C>G | |
| NG_011563.2:g.7403C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000222304.5:c.151-29C>G MANE Select | ENSP00000222304.2:n.151-29C>G | |
| ENST00000222304.3:c.151-29C>G | ENSP00000222304.2:n.151-29C>G | |
| ENST00000593580.1:n.2393C>G | ||
| ENST00000598398.5:c.151-29C>G | ENSP00000471894.1:n.151-29C>G | |
| NM_021175.2:c.151-29C>G | NP_066998.1:n.151-29C>G | |
| NM_021175.3:c.151-29C>G | NP_066998.1:n.151-29C>G | |
| NM_021175.4:c.151-29C>G MANE Select | NP_066998.1:n.151-29C>G |