Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.117263066T>C , CM000672.2:g.117263066T>C | GRCh38 |
| NC_000010.10:g.119022577T>C , CM000672.1:g.119022577T>C | GRCh37 |
| NC_000010.9:g.119012567T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000644641.2:c.992-3667T>C MANE Select | ENSP00000496339.1:n.992-3667T>C | |
| ENST00000298472.9:c.992-3667T>C | ENSP00000298472.5:n.992-3667T>C | |
| ENST00000497497.1:n.1408-3667T>C | ||
| NM_003054.4:c.992-3667T>C | NP_003045.2:n.992-3667T>C | |
| NM_003054.5:c.992-3667T>C | NP_003045.2:n.992-3667T>C | |
| NM_003054.6:c.992-3667T>C MANE Select | NP_003045.2:n.992-3667T>C |