Linked Data
ClinVar Variation Id:
409301
ClinVar RCV Id:
RCV003477969
dbSNP Id:
rs1060502326
gnomAD v4:
17-43063330-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43063330T>C , CM000679.2:g.43063330T>C | GRCh38 |
| NC_000017.10:g.41215347T>C , CM000679.1:g.41215347T>C | GRCh37 |
| NC_000017.9:g.38468873T>C | NCBI36 |
| NG_005905.2:g.154654A>G , LRG_292:g.154654A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000461574.2:c.5190+3A>G | ENSP00000417241.2:n.5190+3A>G | |
| ENST00000470026.6:c.5193+3A>G | ENSP00000419274.2:n.5193+3A>G | |
| ENST00000473961.6:c.5067+3A>G | ENSP00000420201.2:n.5067+3A>G | |
| ENST00000476777.6:c.5187+3A>G | ENSP00000417554.2:n.5187+3A>G | |
| ENST00000477152.6:c.5115+3A>G | ENSP00000419988.2:n.5115+3A>G | |
| ENST00000478531.6:c.1881+3A>G | ENSP00000420412.2:n.1881+3A>G | |
| ENST00000489037.2:c.5115+3A>G | ENSP00000420781.2:n.5115+3A>G | |
| ENST00000493919.6:c.1743+3A>G | ENSP00000418819.2:n.1743+3A>G | |
| ENST00000494123.6:c.5193+3A>G | ENSP00000419103.2:n.5193+3A>G | |
| ENST00000497488.2:c.4305+3A>G | ENSP00000418986.2:n.4305+3A>G | |
| ENST00000618469.2:c.5193+3A>G | ENSP00000478114.2:n.5193+3A>G | |
| ENST00000634433.2:c.5070+3A>G | ENSP00000489431.2:n.5070+3A>G | |
| ENST00000644379.2:c.5259+3A>G | ENSP00000496570.2:n.5259+3A>G | |
| ENST00000644555.2:c.1743+3A>G | ENSP00000494614.2:n.1743+3A>G | |
| ENST00000652672.2:c.5052+3A>G | ENSP00000498906.2:n.5052+3A>G | |
| ENST00000484087.6:c.1755+3A>G | ENSP00000419481.2:n.1755+3A>G | |
| ENST00000357654.9:c.5193+3A>G MANE Select | ENSP00000350283.3:n.5193+3A>G | |
| ENST00000471181.7:c.5256+3A>G | ENSP00000418960.2:n.5256+3A>G | |
| ENST00000644379.1:c.1580+3A>G | ||
| ENST00000352993.7:c.1767+3A>G | ENSP00000312236.5:n.1767+3A>G | |
| ENST00000357654.7:c.5193+3A>G | ENSP00000350283.3:n.5193+3A>G | |
| ENST00000461221.5:c.*4976+3A>G | ENSP00000418548.1:n.*4976+3A>G | |
| ENST00000468300.5:c.1881+3A>G | ENSP00000417148.1:n.1881+3A>G | |
| ENST00000471181.6:c.5256+3A>G | ENSP00000418960.2:n.5256+3A>G | |
| ENST00000491747.6:c.1881+3A>G | ENSP00000420705.2:n.1881+3A>G | |
| ENST00000493795.5:c.5052+3A>G | ENSP00000418775.1:n.5052+3A>G | |
| ENST00000586385.5:c.123+3A>G | ENSP00000465818.1:n.123+3A>G | |
| ENST00000591534.5:c.666+3A>G | ENSP00000467329.1:n.666+3A>G | |
| ENST00000591849.5:c.-98-13140A>G | ENSP00000465347.1:n.-98-13140A>G | |
| NM_007294.3:c.5193+3A>G , LRG_292t1:c.5193+3A>G | NP_009225.1:n.5193+3A>G | |
| NM_007297.3:c.5052+3A>G | NP_009228.2:n.5052+3A>G | |
| NM_007298.3:c.1881+3A>G | NP_009229.2:n.1881+3A>G | |
| NM_007299.3:c.1881+3A>G | NP_009230.2:n.1881+3A>G | |
| NM_007300.3:c.5256+3A>G | NP_009231.2:n.5256+3A>G | |
| NR_027676.1:n.5329+3A>G | ||
| NM_007294.4:c.5193+3A>G MANE Select | NP_009225.1:n.5193+3A>G | |
| NM_007297.4:c.5052+3A>G | NP_009228.2:n.5052+3A>G | |
| NM_007299.4:c.1881+3A>G | NP_009230.2:n.1881+3A>G | |
| NM_007300.4:c.5256+3A>G | NP_009231.2:n.5256+3A>G | |
| NR_027676.2:n.5370+3A>G |