Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.763986G= , CM000673.2:g.763986G= | GRCh38 |
| NC_000011.9:g.763986G= , CM000673.1:g.763986G= | GRCh37 |
| NC_000011.8:g.753986G= | NCBI36 |
| NG_008160.1:g.21555G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000319006.8:c.835+42G= MANE Select | ENSP00000321259.3:n.835+42G= | |
| ENST00000319006.7:c.835+42G= | ENSP00000321259.3:n.835+42G= | |
| ENST00000528097.5:c.831+46G= | ENSP00000437098.1:n.831+46G= | |
| ENST00000530666.1:n.5G= | ||
| NM_006755.1:c.835+42G= | NP_006746.1:n.835+42G= | |
| NM_006755.2:c.835+42G= MANE Select | NP_006746.1:n.835+42G= |