Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.169550066A>G , CM000663.2:g.169550066A>G | GRCh38 |
| NC_000001.10:g.169519304A>G , CM000663.1:g.169519304A>G | GRCh37 |
| NC_000001.9:g.167785928A>G | NCBI36 |
| NG_011806.1:g.41466T>C , LRG_553:g.41466T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000130.5:c.1397-51T>C MANE Select | NP_000121.2:n.1397-51T>C |
| ENST00000367797.9:c.1397-51T>C MANE Select | ENSP00000356771.3:n.1397-51T>C |
| NM_000130.4:c.1397-51T>C , LRG_553t1:c.1397-51T>C | NP_000121.2:n.1397-51T>C |
| ENST00000367796.3:c.1397-51T>C | ENSP00000356770.3:n.1397-51T>C |
| ENST00000367797.7:c.1397-51T>C | ENSP00000356771.3:n.1397-51T>C |
| XM_017000660.2:c.986-51T>C | XP_016856149.1:n.986-51T>C |