Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.52186415G>T , CM000668.2:g.52186415G>T | GRCh38 |
| NC_000006.11:g.52051213G>T , CM000668.1:g.52051213G>T | GRCh37 |
| NC_000006.10:g.52159172G>T | NCBI36 |
| NG_033021.1:g.5029G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000648244.1:c.-17G>T MANE Select | ENSP00000497968.1:n.-17G>T | |
| ENST00000340057.1:c.-17G>T | ENSP00000344192.1:n.-17G>T | |
| NM_002190.2:c.-17G>T | NP_002181.1:n.-17G>T | |
| NM_002190.3:c.-17G>T MANE Select | NP_002181.1:n.-17G>T |