Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.160130615T>C , CM000663.2:g.160130615T>C | GRCh38 |
| NC_000001.10:g.160100405T>C , CM000663.1:g.160100405T>C | GRCh37 |
| NC_000001.9:g.158367029T>C | NCBI36 |
| NG_008014.1:g.19858T>C , LRG_6:g.19858T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361216.8:c.1827+18T>C MANE Select | ENSP00000354490.3:n.1827+18T>C | |
| ENST00000361216.7:c.1827+18T>C | ENSP00000354490.3:n.1827+18T>C | |
| ENST00000392233.7:c.1827+18T>C | ENSP00000376066.3:n.1827+18T>C | |
| ENST00000447527.1:c.959+18T>C | ||
| ENST00000472488.5:n.1930+18T>C | ||
| NM_000702.3:c.1827+18T>C | NP_000693.1:n.1827+18T>C | |
| NM_000702.4:c.1827+18T>C MANE Select | NP_000693.1:n.1827+18T>C |