Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.1401255C= , CM000681.2:g.1401255C= | GRCh38 |
| NC_000019.9:g.1401254C= , CM000681.1:g.1401254C= | GRCh37 |
| NC_000019.8:g.1352254C= | NCBI36 |
| NG_009785.1:g.5299G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252288.8:c.181+41G= MANE Select | ENSP00000252288.1:n.181+41G= | |
| ENST00000447102.8:c.181+41G= | ENSP00000403536.2:n.181+41G= | |
| ENST00000640762.1:c.112+110G= | ENSP00000492031.1:n.112+110G= | |
| ENST00000252288.6:c.181+41G= | ENSP00000252288.1:n.181+41G= | |
| ENST00000447102.7:c.181+41G= | ENSP00000403536.2:n.181+41G= | |
| NM_000156.5:c.181+41G= | NP_000147.1:n.181+41G= | |
| NM_138924.2:c.181+41G= | NP_620279.1:n.181+41G= | |
| NM_000156.6:c.181+41G= MANE Select | NP_000147.1:n.181+41G= | |
| NM_138924.3:c.181+41G= | NP_620279.1:n.181+41G= |