Linked Data
ClinVar Variation Id:
228525
dbSNP Id:
rs748731866
ExAC:
14:31355012 G / A
gnomAD v2:
14-31355012-G-A
gnomAD v3:
14-30885806-G-A
gnomAD v4:
14-30885806-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.30885806G>A , CM000676.2:g.30885806G>A | GRCh38 |
| NC_000014.8:g.31355012G>A , CM000676.1:g.31355012G>A | GRCh37 |
| NC_000014.7:g.30424763G>A | NCBI36 |
| NG_008211.2:g.16272G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000216361.9:c.1166G>A | ENSP00000216361.5:p.Arg389Gln | |
| ENST00000396618.9:c.971G>A MANE Select | ENSP00000379862.3:p.Arg324Gln | |
| ENST00000555117.2:c.1028G>A | ENSP00000493569.1:p.Arg343Gln | |
| ENST00000643575.1:c.971G>A | ENSP00000494838.1:p.Arg324Gln | |
| ENST00000643697.1:n.1273G>A | ||
| ENST00000644874.2:c.971G>A | ENSP00000496360.1:p.Arg324Gln | |
| ENST00000216361.8:c.971G>A | ENSP00000216361.4:p.Arg324Gln | |
| ENST00000396618.7:c.971G>A | ENSP00000379862.3:p.Arg324Gln | |
| ENST00000460581.6:c.635G>A | ENSP00000451713.1:p.Arg212Gln | |
| ENST00000468826.2:c.622G>A | ||
| ENST00000475087.5:c.971G>A | ENSP00000451528.1:p.Arg324Gln | |
| NM_001135058.1:c.971G>A | NP_001128530.1:p.Arg324Gln | |
| NM_004086.2:c.971G>A | NP_004077.1:p.Arg324Gln | |
| NR_038356.1:n.1059C>T | ||
| XM_011536539.1:c.971G>A | XP_011534841.1:p.Arg324Gln | |
| NM_001347720.1:c.1166G>A | NP_001334649.1:p.Arg389Gln | |
| XM_017021071.1:c.1166G>A | XP_016876560.1:p.Arg389Gln | |
| XM_024449506.1:c.1028G>A | XP_024305274.1:p.Arg343Gln | |
| NM_004086.3:c.971G>A MANE Select | NP_004077.1:p.Arg324Gln | |
| NM_001135058.2:c.971G>A | NP_001128530.1:p.Arg324Gln | |
| NM_001347720.2:c.1166G>A | NP_001334649.1:p.Arg389Gln |