Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.71942922T= , CM000674.2:g.71942922T= | GRCh38 |
| NC_000012.11:g.72336702T= , CM000674.1:g.72336702T= | GRCh37 |
| NC_000012.10:g.70622969T= | NCBI36 |
| NG_008279.1:g.9077T= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000333850.4:c.255+1189T= MANE Select | ENSP00000329093.3:n.255+1189T= | |
| ENST00000333850.3:c.255+1189T= | ENSP00000329093.3:n.255+1189T= | |
| ENST00000546576.1:n.265+1189T= | ||
| NM_173353.3:c.255+1189T= | NP_775489.2:n.255+1189T= | |
| XR_245894.2:n.355+1189T= | ||
| XR_001748575.1:n.355+1189T= | ||
| NM_173353.4:c.255+1189T= MANE Select | NP_775489.2:n.255+1189T= |