Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.14871464T= , CM000667.2:g.14871464T= | GRCh38 |
| NC_000005.9:g.14871573T= , CM000667.1:g.14871573T= | GRCh37 |
| NC_000005.8:g.14924573T= | NCBI36 |
| NG_008273.1:g.5315A= | |
| NG_008273.2:g.5322A= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000284268.8:c.-17A= MANE Select | ENSP00000284268.6:n.-17A= | |
| ENST00000284268.6:c.-17A= | ENSP00000284268.6:n.-17A= | |
| ENST00000505140.1:c.-17A= | ENSP00000426332.1:n.-17A= | |
| ENST00000513115.1:n.9A= | ||
| NM_054027.4:c.-17A= | NP_473368.1:n.-17A= | |
| XM_011514067.1:c.-17A= | XP_011512369.1:n.-17A= | |
| NM_054027.5:c.-17A= | NP_473368.1:n.-17A= | |
| NM_054027.6:c.-17A= MANE Select | NP_473368.1:n.-17A= |