Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6709493T>A , CM000681.2:g.6709493T>A | GRCh38 |
| NC_000019.9:g.6709504T>A , CM000681.1:g.6709504T>A | GRCh37 |
| NC_000019.8:g.6660504T>A | NCBI36 |
| NG_009557.1:g.16159A>T , LRG_27:g.16159A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695652.1:c.1722+191A>T | ENSP00000512083.1:n.1722+191A>T | |
| ENST00000695654.1:c.969+191A>T | ENSP00000512085.1:n.969+191A>T | |
| ENST00000695655.1:c.786+191A>T | ENSP00000512086.1:n.786+191A>T | |
| ENST00000695692.1:n.1209+191A>T | ||
| ENST00000245907.11:c.1845+191A>T MANE Select | ENSP00000245907.4:n.1845+191A>T | |
| ENST00000245907.10:c.1845+191A>T | ENSP00000245907.4:n.1845+191A>T | |
| NM_000064.3:c.1845+191A>T | NP_000055.2:n.1845+191A>T | |
| NM_000064.4:c.1845+191A>T MANE Select | NP_000055.2:n.1845+191A>T |