Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.43352215G>T , CM000663.2:g.43352215G>T | GRCh38 |
| NC_000001.10:g.43817886G>T , CM000663.1:g.43817886G>T | GRCh37 |
| NC_000001.9:g.43590473G>T | NCBI36 |
| NG_007525.1:g.19412G>T , LRG_510:g.19412G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005373.3:c.1566-1G>T MANE Select | NP_005364.1:n.1566-1G>T |
| ENST00000372470.9:c.1566-1G>T MANE Select | ENSP00000361548.3:n.1566-1G>T |
| NM_005373.2:c.1566-1G>T , LRG_510t1:c.1566-1G>T | NP_005364.1:n.1566-1G>T |
| ENST00000372470.7:c.1566-1G>T | ENSP00000361548.3:n.1566-1G>T |
| ENST00000413998.7:c.1545-1G>T | ENSP00000414004.3:n.1545-1G>T |
| ENST00000643351.1:c.224-1G>T | |
| XM_011541478.1:c.1545-1G>T | XP_011539780.1:n.1545-1G>T |
| XM_017001320.1:c.1737-1G>T | XP_016856809.1:n.1737-1G>T |