Linked Data
dbSNP Id:
rs753953105
ExAC:
3:14190302 T / C
gnomAD v2:
3-14190302-T-C
gnomAD v3:
3-14148802-T-C
gnomAD v4:
3-14148802-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.14148802T>C , CM000665.2:g.14148802T>C | GRCh38 |
| NC_000003.11:g.14190302T>C , CM000665.1:g.14190302T>C | GRCh37 |
| NC_000003.10:g.14165303T>C | NCBI36 |
| NG_011763.1:g.34871A>G , LRG_472:g.34871A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000285021.12:c.2250+12A>G MANE Select | ENSP00000285021.8:n.2250+12A>G | |
| ENST00000285021.11:c.2250+12A>G | ENSP00000285021.7:n.2250+12A>G | |
| ENST00000427795.2:n.115+12A>G | ||
| ENST00000476581.6:c.*1703+12A>G | ENSP00000424548.1:n.*1703+12A>G | |
| NM_004628.4:c.2250+12A>G , LRG_472t1:c.2250+12A>G | NP_004619.3:n.2250+12A>G | |
| NR_027299.1:n.2230+12A>G | ||
| XM_011534092.1:c.2250+12A>G | XP_011532394.1:n.2250+12A>G | |
| NM_001354726.1:c.1671+12A>G | NP_001341655.1:n.1671+12A>G | |
| NM_001354727.1:c.2244+12A>G | NP_001341656.1:n.2244+12A>G | |
| NM_001354729.1:c.2232+12A>G | NP_001341658.1:n.2232+12A>G | |
| NM_001354730.1:c.2004+12A>G | NP_001341659.1:n.2004+12A>G | |
| NR_148950.1:n.2193+12A>G | ||
| NR_148951.1:n.2069+12A>G | ||
| XR_001740256.2:n.2283+12A>G | ||
| XR_002959580.1:n.2283+12A>G | ||
| XR_002959581.1:n.3900+12A>G | ||
| NM_001354727.2:c.2244+12A>G | NP_001341656.1:n.2244+12A>G | |
| NM_004628.5:c.2250+12A>G MANE Select | NP_004619.3:n.2250+12A>G | |
| NR_148950.2:n.2122+12A>G | ||
| NR_148951.2:n.1998+12A>G | ||
| NM_001354726.2:c.1671+12A>G | NP_001341655.1:n.1671+12A>G | |
| NM_001354729.2:c.2232+12A>G | NP_001341658.1:n.2232+12A>G | |
| NM_001354730.2:c.2004+12A>G | NP_001341659.1:n.2004+12A>G |