Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.44372259C= , CM000679.2:g.44372259C= | GRCh38 |
| NC_000017.10:g.42449627C= , CM000679.1:g.42449627C= | GRCh37 |
| NC_000017.9:g.39805153C= | NCBI36 |
| NG_008331.1:g.22247G= , LRG_479:g.22247G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262407.6:c.*105G= MANE Select | ENSP00000262407.5:n.*105G= | |
| ENST00000648408.1:c.2539G= | ||
| ENST00000262407.5:c.*105G= | ENSP00000262407.5:n.*105G= | |
| ENST00000587295.5:c.418G= | ||
| ENST00000588098.1:c.202G= | ||
| NM_000419.3:c.*105G= , LRG_479t1:c.*105G= | NP_000410.2:n.*105G= | |
| XM_011524749.1:c.*105G= | XP_011523051.1:n.*105G= | |
| XM_011524750.1:c.*105G= | XP_011523052.1:n.*105G= | |
| NM_000419.4:c.*105G= | NP_000410.2:n.*105G= | |
| NM_000419.5:c.*105G= MANE Select | NP_000410.2:n.*105G= |