Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.38409026G= , CM000685.2:g.38409026G= | GRCh38 |
| NC_000023.10:g.38268279G= , CM000685.1:g.38268279G= | GRCh37 |
| NC_000023.9:g.38153223G= | NCBI36 |
| NG_008471.1:g.61544G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000531.6:c.867+1G= MANE Select | NP_000522.3:n.867+1G= |
| ENST00000039007.5:c.867+1G= MANE Select | ENSP00000039007.4:n.867+1G= |
| NM_000531.5:c.867+1G= | NP_000522.3:n.867+1G= |
| ENST00000039007.4:c.867+1G= | ENSP00000039007.4:n.867+1G= |
| ENST00000465127.1:c.172-257095G= | ENSP00000417050.1:n.172-257095G= |
| ENST00000643344.1:c.*617+1G= | ENSP00000496606.1:n.*617+1G= |
| XM_017029556.1:c.867+1G= | XP_016885045.1:n.867+1G= |