Linked Data
ClinVar Variation Id:
868670
ClinVar RCV Id:
RCV001077612
dbSNP Id:
rs772885662
gnomAD v2:
17-41215928-T-C
gnomAD v4:
17-43063911-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43063911T>C , CM000679.2:g.43063911T>C | GRCh38 |
| NC_000017.10:g.41215928T>C , CM000679.1:g.41215928T>C | GRCh37 |
| NC_000017.9:g.38469454T>C | NCBI36 |
| NG_005905.2:g.154073A>G , LRG_292:g.154073A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000461574.2:c.5112A>G | ENSP00000417241.2:p.Leu1704= | |
| ENST00000470026.6:c.5115A>G | ENSP00000419274.2:p.Leu1705= | |
| ENST00000473961.6:c.4989A>G | ENSP00000420201.2:p.Leu1663= | |
| ENST00000476777.6:c.5109A>G | ENSP00000417554.2:p.Leu1703= | |
| ENST00000477152.6:c.5037A>G | ENSP00000419988.2:p.Leu1679= | |
| ENST00000478531.6:c.1803A>G | ENSP00000420412.2:p.Leu601= | |
| ENST00000489037.2:c.5037A>G | ENSP00000420781.2:p.Leu1679= | |
| ENST00000493919.6:c.1665A>G | ENSP00000418819.2:p.Leu555= | |
| ENST00000494123.6:c.5115A>G | ENSP00000419103.2:p.Leu1705= | |
| ENST00000497488.2:c.4227A>G | ENSP00000418986.2:p.Leu1409= | |
| ENST00000618469.2:c.5115A>G | ENSP00000478114.2:p.Leu1705= | |
| ENST00000634433.2:c.4992A>G | ENSP00000489431.2:p.Leu1664= | |
| ENST00000644379.2:c.5181A>G | ENSP00000496570.2:p.Leu1727= | |
| ENST00000644555.2:c.1665A>G | ENSP00000494614.2:p.Leu555= | |
| ENST00000652672.2:c.4974A>G | ENSP00000498906.2:p.Leu1658= | |
| ENST00000484087.6:c.1677A>G | ENSP00000419481.2:p.Leu559= | |
| ENST00000357654.9:c.5115A>G MANE Select | ENSP00000350283.3:p.Leu1705= | |
| ENST00000471181.7:c.5178A>G | ENSP00000418960.2:p.Leu1726= | |
| ENST00000644379.1:c.1502A>G | ||
| ENST00000352993.7:c.1689A>G | ENSP00000312236.5:p.Leu563= | |
| ENST00000357654.7:c.5115A>G | ENSP00000350283.3:p.Leu1705= | |
| ENST00000461221.5:c.*4898A>G | ENSP00000418548.1:n.*4898A>G | |
| ENST00000468300.5:c.1803A>G | ENSP00000417148.1:p.Leu601= | |
| ENST00000471181.6:c.5178A>G | ENSP00000418960.2:p.Leu1726= | |
| ENST00000478531.5:c.1803A>G | ENSP00000420412.1:p.Leu601= | |
| ENST00000484087.5:c.1428A>G | ENSP00000419481.1:p.Leu476= | |
| ENST00000491747.6:c.1803A>G | ENSP00000420705.2:p.Leu601= | |
| ENST00000493795.5:c.4974A>G | ENSP00000418775.1:p.Leu1658= | |
| ENST00000493919.5:c.1665A>G | ENSP00000418819.1:p.Leu555= | |
| ENST00000586385.5:c.45A>G | ENSP00000465818.1:p.Leu15= | |
| ENST00000591534.5:c.588A>G | ENSP00000467329.1:p.Leu196= | |
| ENST00000591849.5:c.-98-13721A>G | ENSP00000465347.1:n.-98-13721A>G | |
| NM_007294.3:c.5115A>G , LRG_292t1:c.5115A>G | NP_009225.1:p.Leu1705= | |
| NM_007297.3:c.4974A>G | NP_009228.2:p.Leu1658= | |
| NM_007298.3:c.1803A>G | NP_009229.2:p.Leu601= | |
| NM_007299.3:c.1803A>G | NP_009230.2:p.Leu601= | |
| NM_007300.3:c.5178A>G | NP_009231.2:p.Leu1726= | |
| NR_027676.1:n.5251A>G | ||
| NM_007294.4:c.5115A>G MANE Select | NP_009225.1:p.Leu1705= | |
| NM_007297.4:c.4974A>G | NP_009228.2:p.Leu1658= | |
| NM_007299.4:c.1803A>G | NP_009230.2:p.Leu601= | |
| NM_007300.4:c.5178A>G | NP_009231.2:p.Leu1726= | |
| NR_027676.2:n.5292A>G |