Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.43838958T= , CM000664.2:g.43838958T= | GRCh38 |
| NC_000002.11:g.44066097T= , CM000664.1:g.44066097T= | GRCh37 |
| NC_000002.10:g.43919601T= | NCBI36 |
| NG_008883.1:g.4862A= | |
| NG_008884.1:g.4995T= | |
| NG_008884.2:g.12017T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000643284.1:n.521-5549T= | ||
| ENST00000644611.1:c.76-5549T= | ENSP00000495423.1:n.76-5549T= | |
| XM_011533029.1:c.76-5549T= | XP_011531331.1:n.76-5549T= | |
| XM_011533030.1:c.76-5549T= | XP_011531332.1:n.76-5549T= | |
| XM_011533031.1:c.-153-5549T= | XP_011531333.1:n.-153-5549T= | |
| XR_939707.1:n.566-5549T= | ||
| XM_011533029.2:c.76-5549T= | XP_011531331.1:n.76-5549T= | |
| XM_011533030.2:c.76-5549T= | XP_011531332.1:n.76-5549T= | |
| XR_001738891.1:n.580-5549T= | ||
| XR_939707.2:n.580-5549T= |