Linked Data
ClinVar Variation Id:
94906
dbSNP Id:
rs112896869
ExAC:
2:238290066 G / A
gnomAD v2:
2-238290066-G-A
gnomAD v3:
2-237381423-G-A
gnomAD v4:
2-237381423-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.237381423G>A , CM000664.2:g.237381423G>A | GRCh38 |
| NC_000002.11:g.238290066G>A , CM000664.1:g.238290066G>A | GRCh37 |
| NC_000002.10:g.237954805G>A | NCBI36 |
| NG_008676.1:g.37785C>T , LRG_473:g.37785C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000353578.9:c.771C>T | ENSP00000315873.4:p.Ala257= | |
| ENST00000682405.1:n.162C>T | ||
| ENST00000295550.9:c.1389C>T MANE Select | ENSP00000295550.4:p.Ala463= | |
| ENST00000295550.8:c.1389C>T | ENSP00000295550.4:p.Ala463= | |
| ENST00000347401.7:c.168C>T | ENSP00000315609.4:p.Ala56= | |
| ENST00000353578.8:c.771C>T | ENSP00000315873.4:p.Ala257= | |
| ENST00000392003.6:c.168C>T | ENSP00000375860.2:p.Ala56= | |
| ENST00000392004.7:c.771C>T | ENSP00000375861.3:p.Ala257= | |
| ENST00000409809.5:c.771C>T | ENSP00000386844.1:p.Ala257= | |
| ENST00000433762.1:c.1389C>T | ENSP00000389539.1:p.Ala463= | |
| ENST00000472056.5:c.168C>T | ENSP00000418285.1:p.Ala56= | |
| NM_004369.3:c.1389C>T , LRG_473t1:c.1389C>T | NP_004360.2:p.Ala463= | |
| NM_057164.4:c.168C>T | NP_476505.3:p.Ala56= | |
| NM_057165.4:c.771C>T | NP_476506.3:p.Ala257= | |
| NM_057166.4:c.168C>T | NP_476507.3:p.Ala56= | |
| NM_057167.3:c.771C>T | NP_476508.2:p.Ala257= | |
| XM_005246065.1:c.1389C>T | XP_005246122.1:p.Ala463= | |
| XM_005246066.1:c.168C>T | XP_005246123.1:p.Ala56= | |
| XM_006712253.1:c.1389C>T | XP_006712316.1:p.Ala463= | |
| XM_011510574.1:c.1389C>T | XP_011508876.1:p.Ala463= | |
| XM_011510575.1:c.92-4079C>T | XP_011508877.1:n.92-4079C>T | |
| XM_017003304.1:c.92-4079C>T | XP_016858793.1:n.92-4079C>T | |
| XM_024452684.1:c.168C>T | XP_024308452.1:p.Ala56= | |
| NM_004369.4:c.1389C>T MANE Select | NP_004360.2:p.Ala463= | |
| NM_057164.5:c.168C>T | NP_476505.3:p.Ala56= | |
| NM_057165.5:c.771C>T | NP_476506.3:p.Ala257= | |
| NM_057166.5:c.168C>T | NP_476507.3:p.Ala56= | |
| NM_057167.4:c.771C>T | NP_476508.2:p.Ala257= |