Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.95324425G= , CM000669.2:g.95324425G= | GRCh38 |
| NC_000007.13:g.94953737G= , CM000669.1:g.94953737G= | GRCh37 |
| NC_000007.12:g.94791673G= | NCBI36 |
| NG_008779.1:g.5148C= | |
| NG_008779.2:g.5282C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000222381.8:c.51C= MANE Select | ENSP00000222381.3:p.Phe17= | |
| ENST00000222381.7:c.51C= | ENSP00000222381.3:p.Phe17= | |
| ENST00000433729.1:c.51C= | ENSP00000407359.1:p.Phe17= | |
| NM_000446.5:c.51C= | NP_000437.3:p.Phe17= | |
| NM_000446.6:c.51C= | NP_000437.3:p.Phe17= | |
| NM_000446.7:c.51C= MANE Select | NP_000437.3:p.Phe17= |