Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.103086458T>C , CM000672.2:g.103086458T>C | GRCh38 |
| NC_000010.10:g.104846215T>C , CM000672.1:g.104846215T>C | GRCh37 |
| NC_000010.9:g.104836205T>C | NCBI36 |
| NG_042272.1:g.111849A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369878.9:c.*9278T>C MANE Select | ENSP00000358894.3:n.*9278T>C | |
| ENST00000369878.8:c.*9278T>C | ENSP00000358894.3:n.*9278T>C | |
| XR_001747118.1:n.12159T>C | ||
| XR_001747121.1:n.12123T>C | ||
| NM_017649.5:c.*9278T>C MANE Select | NP_060119.3:n.*9278T>C | |
| NM_199076.3:c.*9278T>C | NP_951058.1:n.*9278T>C |