Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1411002G= , CM000667.2:g.1411002G= | GRCh38 |
| NC_000005.9:g.1411117G= , CM000667.1:g.1411117G= | GRCh37 |
| NC_000005.8:g.1464117G= | NCBI36 |
| NG_015885.1:g.39427C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270349.12:c.1269+241C= MANE Select | ENSP00000270349.9:n.1269+241C= | |
| ENST00000270349.11:c.1269+241C= | ENSP00000270349.9:n.1269+241C= | |
| NM_001044.4:c.1269+241C= | NP_001035.1:n.1269+241C= | |
| NM_001044.5:c.1269+241C= MANE Select | NP_001035.1:n.1269+241C= |