Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.153615864C= , CM000663.2:g.153615864C= | GRCh38 |
| NC_000001.10:g.153588340C= , CM000663.1:g.153588340C= | GRCh37 |
| NC_000001.9:g.151854964C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344616.4:c.-6G= MANE Select | ENSP00000340463.2:n.-6G= | |
| ENST00000344616.3:c.-6G= | ENSP00000340463.2:n.-6G= | |
| ENST00000368700.7:n.101+4G= | ||
| ENST00000368701.5:c.-6G= | ENSP00000357690.1:n.-6G= | |
| ENST00000368702.5:c.-6G= | ENSP00000357691.1:n.-6G= | |
| ENST00000469571.1:n.148G= | ||
| ENST00000476873.5:c.-6G= | ENSP00000420296.1:n.-6G= | |
| NM_020672.2:c.-6G= | NP_065723.1:n.-6G= | |
| XM_005245362.1:c.-6G= | XP_005245419.1:n.-6G= | |
| XM_017001875.1:c.-6G= | XP_016857364.1:n.-6G= | |
| NM_020672.3:c.-6G= MANE Select | NP_065723.1:n.-6G= |