Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.21881168T= , CM000669.2:g.21881168T= | GRCh38 |
| NC_000007.13:g.21920786T= , CM000669.1:g.21920786T= | GRCh37 |
| NC_000007.12:g.21887311T= | NCBI36 |
| NG_012886.2:g.342954T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000409508.8:c.12387+275T= MANE Select | ENSP00000475939.1:n.12387+275T= | |
| ENST00000328843.10:c.12408+275T= | ENSP00000330671.7:n.12408+275T= | |
| ENST00000409508.7:c.12387+275T= | ENSP00000475939.1:n.12387+275T= | |
| ENST00000620169.4:c.12408+275T= | ENSP00000481693.1:n.12408+275T= | |
| NM_001277115.1:c.12387+275T= | NP_001264044.1:n.12387+275T= | |
| NM_001277115.2:c.12387+275T= MANE Select | NP_001264044.1:n.12387+275T= |