Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94405734C>T , CM000669.2:g.94405734C>T | GRCh38 |
| NC_000007.13:g.94035046C>T , CM000669.1:g.94035046C>T | GRCh37 |
| NC_000007.12:g.93872982C>T | NCBI36 |
| NG_007405.1:g.16174C>T , LRG_2:g.16174C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297268.11:c.540+8C>T MANE Select | ENSP00000297268.6:n.540+8C>T | |
| ENST00000297268.10:c.540+8C>T | ENSP00000297268.6:n.540+8C>T | |
| ENST00000620463.1:c.534+8C>T | ENSP00000477719.1:n.534+8C>T | |
| NM_000089.3:c.540+8C>T , LRG_2t1:c.540+8C>T | NP_000080.2:n.540+8C>T | |
| NM_000089.4:c.540+8C>T MANE Select | NP_000080.2:n.540+8C>T |