Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.2444971T= , CM000673.2:g.2444971T= | GRCh38 |
| NC_000011.9:g.2466201T= , CM000673.1:g.2466201T= | GRCh37 |
| NC_000011.8:g.2422777T= | NCBI36 |
| NG_008935.1:g.4981T= , LRG_287:g.4981T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000496887.7:c.23+263T= | ENSP00000434560.2:n.23+263T= | |
| ENST00000496887.6:c.23+263T= | ENSP00000434560.1:n.23+263T= |