Linked Data
ClinVar Variation Id:
208360
dbSNP Id:
rs796065356
gnomAD v2:
9-35800736-C-G
gnomAD v3:
9-35800739-C-G
gnomAD v4:
9-35800739-C-G
PubMed:
PMID:24471569
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.35800739C>G , CM000671.2:g.35800739C>G | GRCh38 |
| NC_000009.11:g.35800736C>G , CM000671.1:g.35800736C>G | GRCh37 |
| NC_000009.10:g.35790736C>G | NCBI36 |
| NG_009249.1:g.13331C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000448821.6:c.1249C>G | ENSP00000402902.2:p.Gln417Glu | |
| ENST00000685871.1:c.1249C>G | ENSP00000509964.1:p.Gln417Glu | |
| ENST00000686159.1:n.1288C>G | ||
| ENST00000686486.1:n.257C>G | ||
| ENST00000687302.1:n.1335C>G | ||
| ENST00000687357.1:c.1249C>G | ENSP00000509549.1:p.Gln417Glu | |
| ENST00000687625.1:n.404C>G | ||
| ENST00000687787.1:c.1249C>G | ENSP00000509440.1:p.Gln417Glu | |
| ENST00000688201.1:n.1281C>G | ||
| ENST00000688226.1:n.1181C>G | ||
| ENST00000688869.1:n.1555C>G | ||
| ENST00000689788.1:c.1043C>G | ENSP00000508973.1:n.1043C>G | |
| ENST00000689898.1:c.1249C>G | ENSP00000509651.1:p.Gln417Glu | |
| ENST00000690070.1:c.1249C>G | ENSP00000509654.1:p.Gln417Glu | |
| ENST00000690267.1:c.1113C>G | ENSP00000510432.1:n.1113C>G | |
| ENST00000690552.1:n.1110C>G | ||
| ENST00000691138.1:n.1110C>G | ||
| ENST00000691969.1:c.824C>G | ENSP00000510244.1:n.824C>G | |
| ENST00000692232.1:n.2405C>G | ||
| ENST00000692233.1:c.1113C>G | ENSP00000509698.1:n.1113C>G | |
| ENST00000692380.1:n.404C>G | ||
| ENST00000692447.1:n.2361C>G | ||
| ENST00000693094.1:c.1249C>G | ENSP00000510161.1:p.Gln417Glu | |
| ENST00000342694.7:c.1249C>G MANE Select | ENSP00000341083.2:p.Gln417Glu | |
| ENST00000342694.6:c.1249C>G | ENSP00000341083.2:p.Gln417Glu | |
| ENST00000464810.5:n.1249C>G | ||
| NM_003995.3:c.1249C>G | NP_003986.2:p.Gln417Glu | |
| XM_005251478.3:c.1249C>G | XP_005251535.1:p.Gln417Glu | |
| XM_005251479.3:c.262C>G | XP_005251536.1:p.Gln88Glu | |
| XM_006716778.2:c.1249C>G | XP_006716841.1:p.Gln417Glu | |
| XM_011517889.1:c.262C>G | XP_011516191.1:p.Gln88Glu | |
| XM_011517890.1:c.262C>G | XP_011516192.1:p.Gln88Glu | |
| XM_011517891.1:c.262C>G | XP_011516193.1:p.Gln88Glu | |
| XM_011517892.1:c.262C>G | XP_011516194.1:p.Gln88Glu | |
| XM_011517893.1:c.262C>G | XP_011516195.1:p.Gln88Glu | |
| XM_011517894.1:c.262C>G | XP_011516196.1:p.Gln88Glu | |
| XM_024447556.1:c.1249C>G | XP_024303324.1:p.Gln417Glu | |
| XM_024447557.1:c.1249C>G | XP_024303325.1:p.Gln417Glu | |
| XM_024447558.1:c.262C>G | XP_024303326.1:p.Gln88Glu | |
| XM_024447560.1:c.-160C>G | XP_024303328.1:n.-160C>G | |
| XM_024447561.1:c.-160C>G | XP_024303329.1:n.-160C>G | |
| NM_003995.4:c.1249C>G MANE Select | NP_003986.2:p.Gln417Glu | |
| NM_001378923.1:c.1249C>G | NP_001365852.1:p.Gln417Glu |