Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.147132382T= , CM000669.2:g.147132382T= | GRCh38 |
| NC_000007.13:g.146829474T= , CM000669.1:g.146829474T= | GRCh37 |
| NC_000007.12:g.146460407T= | NCBI36 |
| NG_007092.2:g.1021022T= | |
| NG_007092.3:g.1021382T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361727.8:c.1221T= MANE Select | ENSP00000354778.3:p.Asn407= | |
| ENST00000636561.1:n.1124T= | ||
| ENST00000636870.1:n.1083T= | ||
| ENST00000637150.1:n.1150T= | ||
| ENST00000637694.1:n.1124T= | ||
| ENST00000637825.1:n.704T= | ||
| ENST00000638117.1:n.1124T= | ||
| ENST00000361727.7:c.1221T= | ENSP00000354778.3:p.Asn407= | |
| NM_014141.5:c.1221T= | NP_054860.1:p.Asn407= | |
| XM_017011950.2:c.1221T= | XP_016867439.1:p.Asn407= | |
| NM_014141.6:c.1221T= MANE Select | NP_054860.1:p.Asn407= |