Linked Data
dbSNP Id:
rs573904407
gnomAD v2:
17-41213928-T-G
gnomAD v3:
17-43061911-T-G
gnomAD v4:
17-43061911-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43061911T>G , CM000679.2:g.43061911T>G | GRCh38 |
| NC_000017.10:g.41213928T>G , CM000679.1:g.41213928T>G | GRCh37 |
| NC_000017.9:g.38467454T>G | NCBI36 |
| NG_005905.2:g.156073A>C , LRG_292:g.156073A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000461574.2:c.5190+1422A>C | ENSP00000417241.2:n.5190+1422A>C | |
| ENST00000470026.6:c.5193+1422A>C | ENSP00000419274.2:n.5193+1422A>C | |
| ENST00000473961.6:c.5067+1422A>C | ENSP00000420201.2:n.5067+1422A>C | |
| ENST00000476777.6:c.5187+1422A>C | ENSP00000417554.2:n.5187+1422A>C | |
| ENST00000477152.6:c.5115+1422A>C | ENSP00000419988.2:n.5115+1422A>C | |
| ENST00000478531.6:c.1881+1422A>C | ENSP00000420412.2:n.1881+1422A>C | |
| ENST00000489037.2:c.5115+1422A>C | ENSP00000420781.2:n.5115+1422A>C | |
| ENST00000493919.6:c.1743+1422A>C | ENSP00000418819.2:n.1743+1422A>C | |
| ENST00000494123.6:c.5193+1422A>C | ENSP00000419103.2:n.5193+1422A>C | |
| ENST00000497488.2:c.4305+1422A>C | ENSP00000418986.2:n.4305+1422A>C | |
| ENST00000618469.2:c.5193+1422A>C | ENSP00000478114.2:n.5193+1422A>C | |
| ENST00000634433.2:c.5070+1422A>C | ENSP00000489431.2:n.5070+1422A>C | |
| ENST00000644379.2:c.5259+1422A>C | ENSP00000496570.2:n.5259+1422A>C | |
| ENST00000644555.2:c.1743+1422A>C | ENSP00000494614.2:n.1743+1422A>C | |
| ENST00000652672.2:c.5052+1422A>C | ENSP00000498906.2:n.5052+1422A>C | |
| ENST00000484087.6:c.1755+1422A>C | ENSP00000419481.2:n.1755+1422A>C | |
| ENST00000357654.9:c.5193+1422A>C MANE Select | ENSP00000350283.3:n.5193+1422A>C | |
| ENST00000471181.7:c.5256+1422A>C | ENSP00000418960.2:n.5256+1422A>C | |
| ENST00000644379.1:c.1580+1422A>C | ||
| ENST00000352993.7:c.1767+1422A>C | ENSP00000312236.5:n.1767+1422A>C | |
| ENST00000357654.7:c.5193+1422A>C | ENSP00000350283.3:n.5193+1422A>C | |
| ENST00000461221.5:c.*4976+1422A>C | ENSP00000418548.1:n.*4976+1422A>C | |
| ENST00000468300.5:c.1881+1422A>C | ENSP00000417148.1:n.1881+1422A>C | |
| ENST00000471181.6:c.5256+1422A>C | ENSP00000418960.2:n.5256+1422A>C | |
| ENST00000491747.6:c.1881+1422A>C | ENSP00000420705.2:n.1881+1422A>C | |
| ENST00000493795.5:c.5052+1422A>C | ENSP00000418775.1:n.5052+1422A>C | |
| ENST00000586385.5:c.123+1422A>C | ENSP00000465818.1:n.123+1422A>C | |
| ENST00000591534.5:c.666+1422A>C | ENSP00000467329.1:n.666+1422A>C | |
| ENST00000591849.5:c.-98-11721A>C | ENSP00000465347.1:n.-98-11721A>C | |
| NM_007294.3:c.5193+1422A>C , LRG_292t1:c.5193+1422A>C | NP_009225.1:n.5193+1422A>C | |
| NM_007297.3:c.5052+1422A>C | NP_009228.2:n.5052+1422A>C | |
| NM_007298.3:c.1881+1422A>C | NP_009229.2:n.1881+1422A>C | |
| NM_007299.3:c.1881+1422A>C | NP_009230.2:n.1881+1422A>C | |
| NM_007300.3:c.5256+1422A>C | NP_009231.2:n.5256+1422A>C | |
| NR_027676.1:n.5329+1422A>C | ||
| NM_007294.4:c.5193+1422A>C MANE Select | NP_009225.1:n.5193+1422A>C | |
| NM_007297.4:c.5052+1422A>C | NP_009228.2:n.5052+1422A>C | |
| NM_007299.4:c.1881+1422A>C | NP_009230.2:n.1881+1422A>C | |
| NM_007300.4:c.5256+1422A>C | NP_009231.2:n.5256+1422A>C | |
| NR_027676.2:n.5370+1422A>C |