Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.121303369C= , CM000673.2:g.121303369C= | GRCh38 |
| NC_000011.9:g.121174078C= , CM000673.1:g.121174078C= | GRCh37 |
| NC_000011.8:g.120679288C= | NCBI36 |
| NG_009446.1:g.15691C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264027.9:c.-7C= MANE Select | ENSP00000264027.4:n.-7C= | |
| ENST00000264027.8:c.-7C= | ENSP00000264027.4:n.-7C= | |
| ENST00000392789.2:c.-7C= | ENSP00000376539.2:n.-7C= | |
| ENST00000524683.5:n.50C= | ||
| ENST00000527762.5:c.-7C= | ENSP00000436290.1:n.-7C= | |
| ENST00000531140.1:n.62C= | ||
| ENST00000534230.5:c.-7C= | ENSP00000432550.1:n.-7C= | |
| ENST00000534455.5:n.140C= | ||
| NM_001024956.2:c.-7C= | NP_001020127.1:n.-7C= | |
| NM_006918.4:c.-7C= | NP_008849.2:n.-7C= | |
| NM_006918.5:c.-7C= MANE Select | NP_008849.2:n.-7C= | |
| NM_001024956.3:c.-7C= | NP_001020127.1:n.-7C= |