Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.103086299T= , CM000672.2:g.103086299T= | GRCh38 |
| NC_000010.10:g.104846056T= , CM000672.1:g.104846056T= | GRCh37 |
| NC_000010.9:g.104836046T= | NCBI36 |
| NG_042272.1:g.112008A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369878.9:c.*9119T= MANE Select | ENSP00000358894.3:n.*9119T= | |
| ENST00000369878.8:c.*9119T= | ENSP00000358894.3:n.*9119T= | |
| XR_001747118.1:n.12000T= | ||
| XR_001747121.1:n.11964T= | ||
| NM_017649.5:c.*9119T= MANE Select | NP_060119.3:n.*9119T= | |
| NM_199076.3:c.*9119T= | NP_951058.1:n.*9119T= |