Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.50130440A= , CM000676.2:g.50130440A= | GRCh38 |
| NC_000014.8:g.50597158A= , CM000676.1:g.50597158A= | GRCh37 |
| NC_000014.7:g.49666908A= | NCBI36 |
| NG_051073.1:g.106254T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000216373.10:c.3337+61T= MANE Select | ENSP00000216373.5:n.3337+61T= | |
| ENST00000216373.9:c.3337+61T= | ENSP00000216373.5:n.3337+61T= | |
| ENST00000543680.5:c.3238+61T= | ENSP00000445328.1:n.3238+61T= | |
| NM_006939.2:c.3337+61T= | NP_008870.2:n.3337+61T= | |
| XM_005268021.1:c.3157+61T= | XP_005268078.1:n.3157+61T= | |
| XM_011537103.1:c.3298+61T= | XP_011535405.1:n.3298+61T= | |
| NM_006939.3:c.3337+61T= | NP_008870.2:n.3337+61T= | |
| NM_006939.4:c.3337+61T= MANE Select | NP_008870.2:n.3337+61T= |