Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.111071858G>T , CM000667.2:g.111071858G>T | GRCh38 |
| NC_000005.9:g.110407556G>T , CM000667.1:g.110407556G>T | GRCh37 |
| NC_000005.8:g.110435455G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344895.4:c.-33G>T MANE Select | ENSP00000339804.3:n.-33G>T | |
| ENST00000344895.3:c.-33G>T | ENSP00000339804.3:n.-33G>T | |
| ENST00000420978.6:c.35-67G>T | ENSP00000399099.2:n.35-67G>T | |
| NM_033035.4:c.-33G>T | NP_149024.1:n.-33G>T | |
| NR_045089.1:n.1439-67G>T | ||
| NM_033035.5:c.-33G>T MANE Select | NP_149024.1:n.-33G>T | |
| NR_045089.2:n.1457-67G>T |