Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.6775501G= , CM000682.2:g.6775501G= | GRCh38 |
| NC_000020.10:g.6756148G= , CM000682.1:g.6756148G= | GRCh37 |
| NC_000020.9:g.6704148G= | NCBI36 |
| NG_023233.1:g.12404G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001200.4:c.347-2744G= MANE Select | NP_001191.1:n.347-2744G= |
| ENST00000378827.5:c.347-2744G= MANE Select | ENSP00000368104.3:n.347-2744G= |
| NM_001200.2:c.347-2744G= | NP_001191.1:n.347-2744G= |
| NM_001200.3:c.347-2744G= | NP_001191.1:n.347-2744G= |
| ENST00000378827.4:c.347-2744G= | ENSP00000368104.3:n.347-2744G= |
| XM_011529323.1:c.-122-2744G= | XP_011527625.1:n.-122-2744G= |