Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6713628G>A , CM000681.2:g.6713628G>A | GRCh38 |
| NC_000019.9:g.6713639G>A , CM000681.1:g.6713639G>A | GRCh37 |
| NC_000019.8:g.6664639G>A | NCBI36 |
| NG_009557.1:g.12024C>T , LRG_27:g.12024C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695652.1:c.651-119C>T | ENSP00000512083.1:n.651-119C>T | |
| ENST00000245907.11:c.774-119C>T MANE Select | ENSP00000245907.4:n.774-119C>T | |
| ENST00000245907.10:c.774-119C>T | ENSP00000245907.4:n.774-119C>T | |
| ENST00000595577.1:n.278-119C>T | ||
| ENST00000597442.5:n.24-119C>T | ||
| NM_000064.3:c.774-119C>T | NP_000055.2:n.774-119C>T | |
| NM_000064.4:c.774-119C>T MANE Select | NP_000055.2:n.774-119C>T |