Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.74493366A= , CM000676.2:g.74493366A= | GRCh38 |
| NC_000014.8:g.74960069A= , CM000676.1:g.74960069A= | GRCh37 |
| NC_000014.7:g.74029822A= | NCBI36 |
| NG_007117.1:g.5016T= | |
| NG_033074.1:g.4647A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000555592.1:c.-63-29T= | ENSP00000450887.1:n.-63-29T= | |
| ENST00000555619.5:c.-92T= | ENSP00000451112.1:n.-92T= | |
| ENST00000556009.5:c.147+665T= | ||
| NM_006432.3:c.-92T= | NP_006423.1:n.-92T= | |
| NM_001363688.1:c.-92T= | NP_001350617.1:n.-92T= | |
| NM_006432.4:c.-92T= | NP_006423.1:n.-92T= |