Linked Data
ClinVar Variation Id:
450952
dbSNP Id:
rs1490746741
gnomAD v2:
11-22249121-A-G
gnomAD v3:
11-22227575-A-G
gnomAD v4:
11-22227575-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.22227575A>G , CM000673.2:g.22227575A>G | GRCh38 |
| NC_000011.9:g.22249121A>G , CM000673.1:g.22249121A>G | GRCh37 |
| NC_000011.8:g.22205697A>G | NCBI36 |
| NG_015844.1:g.39400A>G , LRG_868:g.39400A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682266.1:c.187A>G | ENSP00000507766.1:p.Arg63Gly | |
| ENST00000682341.1:c.595A>G | ENSP00000508251.1:p.Arg199Gly | |
| ENST00000682530.1:c.*569A>G | ENSP00000506805.1:n.*569A>G | |
| ENST00000682684.1:n.1016A>G | ||
| ENST00000683197.1:c.595A>G | ENSP00000507641.1:p.Arg199Gly | |
| ENST00000683411.1:c.187A>G | ENSP00000508397.1:p.Arg63Gly | |
| ENST00000683437.1:c.187A>G | ENSP00000508408.1:p.Arg63Gly | |
| ENST00000683613.1:n.1631A>G | ||
| ENST00000683834.1:n.837A>G | ||
| ENST00000684663.1:c.592A>G | ENSP00000508009.1:p.Arg198Gly | |
| ENST00000324559.9:c.637A>G MANE Select | ENSP00000315371.9:p.Arg213Gly | |
| ENST00000648804.1:n.1202A>G | ||
| ENST00000324559.8:c.637A>G | ENSP00000315371.8:p.Arg213Gly | |
| NM_001142649.1:c.634A>G | NP_001136121.1:p.Arg212Gly | |
| NM_213599.2:c.637A>G , LRG_868t1:c.637A>G | NP_998764.1:p.Arg213Gly | |
| XM_005252820.2:c.595A>G | XP_005252877.2:p.Arg199Gly | |
| XM_005252821.2:c.592A>G | XP_005252878.2:p.Arg198Gly | |
| XM_005252822.3:c.559A>G | XP_005252879.1:p.Arg187Gly | |
| XM_005252823.3:c.556A>G | XP_005252880.1:p.Arg186Gly | |
| XM_011519949.1:c.544A>G | XP_011518251.1:p.Arg182Gly | |
| XM_005252820.3:c.595A>G | XP_005252877.2:p.Arg199Gly | |
| XM_005252821.3:c.592A>G | XP_005252878.2:p.Arg198Gly | |
| XM_005252822.4:c.559A>G | XP_005252879.1:p.Arg187Gly | |
| XM_011519949.2:c.544A>G | XP_011518251.1:p.Arg182Gly | |
| NM_001142649.2:c.634A>G | NP_001136121.1:p.Arg212Gly | |
| NM_213599.3:c.637A>G MANE Select | NP_998764.1:p.Arg213Gly |