Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.28845217A>G , CM000678.2:g.28845217A>G | GRCh38 |
| NC_000016.9:g.28856538A>G , CM000678.1:g.28856538A>G | GRCh37 |
| NC_000016.8:g.28764039A>G | NCBI36 |
| NG_008964.1:g.6192T>C | |
| NG_029706.2:g.3618A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000313511.8:c.414+97T>C MANE Select | ENSP00000322439.3:n.414+97T>C | |
| ENST00000313511.7:c.414+97T>C | ENSP00000322439.3:n.414+97T>C | |
| ENST00000565012.1:c.248-162T>C | ENSP00000455007.1:n.248-162T>C | |
| NM_003321.4:c.414+97T>C | NP_003312.3:n.414+97T>C | |
| XM_011545928.1:c.414+97T>C | XP_011544230.1:n.414+97T>C | |
| NM_001365360.1:c.414+97T>C | NP_001352289.1:n.414+97T>C | |
| NM_003321.5:c.414+97T>C MANE Select | NP_003312.3:n.414+97T>C | |
| NM_001365360.2:c.414+97T>C | NP_001352289.1:n.414+97T>C |