Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.19570371T>C , CM000686.2:g.19570371T>C | GRCh38 |
| NC_000024.9:g.21732257T>C , CM000686.1:g.21732257T>C | GRCh37 |
| NC_000024.8:g.20191645T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000686158.1:n.199+2801T>C | ||
| ENST00000686905.1:n.133+2889T>C | ||
| ENST00000693214.1:n.221+2801T>C | ||
| ENST00000445715.6:n.101+2889T>C | ||
| ENST00000407724.7:n.170+2889T>C | ||
| ENST00000445715.5:n.101+2889T>C | ||
| ENST00000447202.2:n.123+2420T>C | ||
| ENST00000447520.5:n.101+2889T>C | ||
| ENST00000459719.6:n.221+2801T>C | ||
| ENST00000538014.2:n.240+912T>C | ||
| NR_045128.1:n.125+2889T>C | ||
| NR_045129.1:n.125+2889T>C |