Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.102239027C= , CM000670.2:g.102239027C= | GRCh38 |
| NC_000008.10:g.103251255C= , CM000670.1:g.103251255C= | GRCh37 |
| NC_000008.9:g.103320431C= | NCBI36 |
| NG_016617.1:g.5092G= , LRG_788:g.5092G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251810.7:c.-153G= | ENSP00000251810.3:n.-153G= | |
| NM_001172478.1:c.-153G= | NP_001165949.1:n.-153G= | |
| NM_015713.4:c.-153G= , LRG_788t2:c.-153G= | NP_056528.2:n.-153G= |