Linked Data
ClinVar Variation Id:
300469
dbSNP Id:
rs886047142
gnomAD v2:
10-73569846-C-T
gnomAD v3:
10-71810089-C-T
gnomAD v4:
10-71810089-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.71810089C>T , CM000672.2:g.71810089C>T | GRCh38 |
| NC_000010.10:g.73569846C>T , CM000672.1:g.73569846C>T | GRCh37 |
| NC_000010.9:g.73239852C>T | NCBI36 |
| NG_008835.1:g.418143C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000224721.12:c.8979+13C>T MANE Select | ENSP00000224721.9:n.8979+13C>T | |
| ENST00000642965.1:c.2912+13C>T | ENSP00000495222.1:n.2912+13C>T | |
| ENST00000647092.1:c.2576+13C>T | ENSP00000495176.1:n.2576+13C>T | |
| ENST00000224721.10:c.8994+13C>T | ENSP00000224721.8:n.8994+13C>T | |
| ENST00000398788.4:c.2259+13C>T | ENSP00000381768.3:n.2259+13C>T | |
| ENST00000475158.1:n.2515+13C>T | ||
| ENST00000619887.4:c.2259+13C>T | ENSP00000478374.1:n.2259+13C>T | |
| ENST00000622827.4:c.8979+13C>T | ENSP00000483211.1:n.8979+13C>T | |
| NM_001171933.1:c.2259+13C>T | NP_001165404.1:n.2259+13C>T | |
| NM_001171934.1:c.2259+13C>T | NP_001165405.1:n.2259+13C>T | |
| NM_022124.5:c.8979+13C>T | NP_071407.4:n.8979+13C>T | |
| XM_006717940.2:c.9174+13C>T | XP_006718003.1:n.9174+13C>T | |
| XM_006717942.2:c.9108+13C>T | XP_006718005.1:n.9108+13C>T | |
| XM_011540039.1:c.9171+13C>T | XP_011538341.1:n.9171+13C>T | |
| XM_011540040.1:c.9168+13C>T | XP_011538342.1:n.9168+13C>T | |
| XM_011540041.1:c.9114+13C>T | XP_011538343.1:n.9114+13C>T | |
| XM_011540042.1:c.9084+13C>T | XP_011538344.1:n.9084+13C>T | |
| XM_011540043.1:c.9174+13C>T | XP_011538345.1:n.9174+13C>T | |
| XM_011540044.1:c.9039+13C>T | XP_011538346.1:n.9039+13C>T | |
| XM_011540045.1:c.9174+13C>T | XP_011538347.1:n.9174+13C>T | |
| XM_011540046.1:c.8634+13C>T | XP_011538348.1:n.8634+13C>T | |
| XM_011540047.1:c.7992+13C>T | XP_011538349.1:n.7992+13C>T | |
| XM_011540052.1:c.5502+13C>T | XP_011538354.1:n.5502+13C>T | |
| NM_022124.6:c.8979+13C>T MANE Select | NP_071407.4:n.8979+13C>T |