Linked Data
dbSNP Id:
rs767343111
ExAC:
3:14190284 G / A
gnomAD v2:
3-14190284-G-A
gnomAD v3:
3-14148784-G-A
gnomAD v4:
3-14148784-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.14148784G>A , CM000665.2:g.14148784G>A | GRCh38 |
| NC_000003.11:g.14190284G>A , CM000665.1:g.14190284G>A | GRCh37 |
| NC_000003.10:g.14165285G>A | NCBI36 |
| NG_011763.1:g.34889C>T , LRG_472:g.34889C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000285021.12:c.2250+30C>T MANE Select | ENSP00000285021.8:n.2250+30C>T | |
| ENST00000285021.11:c.2250+30C>T | ENSP00000285021.7:n.2250+30C>T | |
| ENST00000427795.2:n.115+30C>T | ||
| ENST00000476581.6:c.*1703+30C>T | ENSP00000424548.1:n.*1703+30C>T | |
| NM_004628.4:c.2250+30C>T , LRG_472t1:c.2250+30C>T | NP_004619.3:n.2250+30C>T | |
| NR_027299.1:n.2230+30C>T | ||
| XM_011534092.1:c.2250+30C>T | XP_011532394.1:n.2250+30C>T | |
| NM_001354726.1:c.1671+30C>T | NP_001341655.1:n.1671+30C>T | |
| NM_001354727.1:c.2244+30C>T | NP_001341656.1:n.2244+30C>T | |
| NM_001354729.1:c.2232+30C>T | NP_001341658.1:n.2232+30C>T | |
| NM_001354730.1:c.2004+30C>T | NP_001341659.1:n.2004+30C>T | |
| NR_148950.1:n.2193+30C>T | ||
| NR_148951.1:n.2069+30C>T | ||
| XR_001740256.2:n.2283+30C>T | ||
| XR_002959580.1:n.2283+30C>T | ||
| XR_002959581.1:n.3900+30C>T | ||
| NM_001354727.2:c.2244+30C>T | NP_001341656.1:n.2244+30C>T | |
| NM_004628.5:c.2250+30C>T MANE Select | NP_004619.3:n.2250+30C>T | |
| NR_148950.2:n.2122+30C>T | ||
| NR_148951.2:n.1998+30C>T | ||
| NM_001354726.2:c.1671+30C>T | NP_001341655.1:n.1671+30C>T | |
| NM_001354729.2:c.2232+30C>T | NP_001341658.1:n.2232+30C>T | |
| NM_001354730.2:c.2004+30C>T | NP_001341659.1:n.2004+30C>T |