Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.74493484T= , CM000676.2:g.74493484T= | GRCh38 |
| NC_000014.8:g.74960187T= , CM000676.1:g.74960187T= | GRCh37 |
| NC_000014.7:g.74029940T= | NCBI36 |
| NG_007117.1:g.4898A= | |
| NG_033074.1:g.4765T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000555592.1:c.-64+86A= | ENSP00000450887.1:n.-64+86A= | |
| ENST00000555619.5:c.-210A= | ENSP00000451112.1:n.-210A= | |
| ENST00000556009.5:c.147+547A= | ||
| NM_001363688.1:c.-210A= | NP_001350617.1:n.-210A= | |
| NM_006432.4:c.-210A= | NP_006423.1:n.-210A= |