Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.95321372A= , CM000669.2:g.95321372A= | GRCh38 |
| NC_000007.13:g.94950684A= , CM000669.1:g.94950684A= | GRCh37 |
| NC_000007.12:g.94788620A= | NCBI36 |
| NG_008779.1:g.8201T= | |
| NG_008779.2:g.8335T= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000222381.8:c.75-2979T= MANE Select | ENSP00000222381.3:n.75-2979T= | |
| ENST00000222381.7:c.75-2979T= | ENSP00000222381.3:n.75-2979T= | |
| ENST00000433729.1:c.75-2979T= | ENSP00000407359.1:n.75-2979T= | |
| NM_000446.5:c.75-2979T= | NP_000437.3:n.75-2979T= | |
| NM_000446.6:c.75-2979T= | NP_000437.3:n.75-2979T= | |
| NM_000446.7:c.75-2979T= MANE Select | NP_000437.3:n.75-2979T= |