Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.61392362T= , CM000673.2:g.61392362T= | GRCh38 |
| NC_000011.9:g.61159834T= , CM000673.1:g.61159834T= | GRCh37 |
| NC_000011.8:g.60916410T= | NCBI36 |
| NG_032976.1:g.5003T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000334888.9:c.-270T= | ENSP00000334844.5:n.-270T= | |
| ENST00000515837.6:c.-270T= | ENSP00000440638.1:n.-270T= | |
| NM_001173990.2:c.-270T= | NP_001167461.1:n.-270T= | |
| NM_001173991.2:c.-270T= | NP_001167462.1:n.-270T= | |
| XM_005274039.3:c.-601T= | XP_005274096.1:n.-601T= | |
| NM_001330285.1:c.-467T= | NP_001317214.1:n.-467T= | |
| XM_005274039.4:c.-601T= | XP_005274096.1:n.-601T= |