Linked Data
ClinVar Variation Id:
434951
dbSNP Id:
rs371855601
ExAC:
2:25457292 G / A
gnomAD v2:
2-25457292-G-A
gnomAD v3:
2-25234423-G-A
gnomAD v4:
2-25234423-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.25234423G>A , CM000664.2:g.25234423G>A | GRCh38 |
| NC_000002.11:g.25457292G>A , CM000664.1:g.25457292G>A | GRCh37 |
| NC_000002.10:g.25310796G>A | NCBI36 |
| NG_029465.2:g.113168C>T , LRG_459:g.113168C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000474887.6:c.847-3C>T | ||
| ENST00000683393.1:c.1744-3C>T | ENSP00000508654.1:n.1744-3C>T | |
| ENST00000683760.1:c.1929-3C>T | ENSP00000507765.1:n.1929-3C>T | |
| ENST00000321117.10:c.2598-3C>T MANE Select | ENSP00000324375.5:n.2598-3C>T | |
| ENST00000264709.7:c.2598-3C>T | ENSP00000264709.3:n.2598-3C>T | |
| ENST00000321117.9:c.2598-3C>T | ENSP00000324375.5:n.2598-3C>T | |
| ENST00000380746.8:c.2031-3C>T | ENSP00000370122.4:n.2031-3C>T | |
| ENST00000380756.7:c.*451-3C>T | ENSP00000370132.3:n.*451-3C>T | |
| ENST00000402667.1:c.1929-3C>T | ENSP00000384237.1:n.1929-3C>T | |
| NM_022552.4:c.2598-3C>T , LRG_459t1:c.2598-3C>T | NP_072046.2:n.2598-3C>T | |
| NM_153759.3:c.2031-3C>T , LRG_459t2:c.2031-3C>T | NP_715640.2:n.2031-3C>T | |
| NM_175629.2:c.2598-3C>T , LRG_459t4:c.2598-3C>T | NP_783328.1:n.2598-3C>T | |
| XM_005264175.3:c.2598-3C>T | XP_005264232.1:n.2598-3C>T | |
| XM_005264177.3:c.1929-3C>T | XP_005264234.1:n.1929-3C>T | |
| XM_006711958.2:c.2154-3C>T | XP_006712021.1:n.2154-3C>T | |
| XM_011532662.1:c.2451-3C>T | XP_011530964.1:n.2451-3C>T | |
| XM_011532663.1:c.2433-3C>T | XP_011530965.1:n.2433-3C>T | |
| XM_011532665.1:c.2142-3C>T | XP_011530967.1:n.2142-3C>T | |
| XM_011532666.1:c.2070-3C>T | XP_011530968.1:n.2070-3C>T | |
| XM_011532667.1:c.1929-3C>T | XP_011530969.1:n.1929-3C>T | |
| NM_001320893.1:c.2142-3C>T | NP_001307822.1:n.2142-3C>T | |
| NR_135490.1:n.3135-3C>T | ||
| XM_005264175.5:c.2598-3C>T | XP_005264232.1:n.2598-3C>T | |
| XM_005264177.4:c.1929-3C>T | XP_005264234.1:n.1929-3C>T | |
| XM_011532662.2:c.2451-3C>T | XP_011530964.1:n.2451-3C>T | |
| XM_011532663.2:c.2433-3C>T | XP_011530965.1:n.2433-3C>T | |
| XM_011532666.2:c.2070-3C>T | XP_011530968.1:n.2070-3C>T | |
| XM_011532667.3:c.1929-3C>T | XP_011530969.1:n.1929-3C>T | |
| XM_017003526.1:c.2598-3C>T | XP_016859015.1:n.2598-3C>T | |
| XM_017003527.1:c.1929-3C>T | XP_016859016.1:n.1929-3C>T | |
| XR_001738657.1:n.2805-3C>T | ||
| NM_001375819.1:c.1929-3C>T | NP_001362748.1:n.1929-3C>T | |
| NR_135490.2:n.3028-3C>T | ||
| NM_022552.5:c.2598-3C>T MANE Select | NP_072046.2:n.2598-3C>T |