Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.46376904C>T , CM000664.2:g.46376904C>T | GRCh38 |
| NC_000002.11:g.46604043C>T , CM000664.1:g.46604043C>T | GRCh37 |
| NC_000002.10:g.46457547C>T | NCBI36 |
| NG_016000.1:g.84503C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263734.5:c.1249+151C>T MANE Select | ENSP00000263734.3:n.1249+151C>T | |
| ENST00000263734.4:c.1249+151C>T | ENSP00000263734.3:n.1249+151C>T | |
| ENST00000483692.1:n.417+151C>T | ||
| NM_001430.4:c.1249+151C>T | NP_001421.2:n.1249+151C>T | |
| XM_011532698.1:c.1288+151C>T | XP_011531000.1:n.1288+151C>T | |
| XM_011532698.2:c.1288+151C>T | XP_011531000.1:n.1288+151C>T | |
| NM_001430.5:c.1249+151C>T MANE Select | NP_001421.2:n.1249+151C>T |