Linked Data
ClinVar Variation Id:
524764
dbSNP Id:
rs768010078
ExAC:
15:91354482 G / A
gnomAD v2:
15-91354482-G-A
gnomAD v3:
15-90811252-G-A
gnomAD v4:
15-90811252-G-A
COSMIC:
COSM4057912
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.90811252G>A , CM000677.2:g.90811252G>A | GRCh38 |
| NC_000015.9:g.91354482G>A , CM000677.1:g.91354482G>A | GRCh37 |
| NC_000015.8:g.89155486G>A | NCBI36 |
| NG_007272.1:g.98881G>A , LRG_20:g.98881G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355112.8:c.3922G>A MANE Select | ENSP00000347232.3:p.Gly1308Arg | |
| ENST00000560559.2:n.2495G>A | ||
| ENST00000648453.1:c.3922G>A | ENSP00000497646.1:p.Gly1308Arg | |
| ENST00000680772.1:c.3922G>A | ENSP00000506117.1:p.Gly1308Arg | |
| ENST00000681142.1:c.3922G>A | ENSP00000506682.1:p.Gly1308Arg | |
| ENST00000355112.7:c.3922G>A | ENSP00000347232.3:p.Gly1308Arg | |
| ENST00000558825.5:n.1269G>A | ||
| ENST00000559724.5:c.*2846G>A | ENSP00000453359.1:n.*2846G>A | |
| ENST00000560136.5:n.1948G>A | ||
| ENST00000560509.5:c.3529G>A | ENSP00000454158.1:p.Gly1177Arg | |
| ENST00000560821.1:n.342G>A | ||
| NM_000057.3:c.3922G>A | NP_000048.1:p.Gly1308Arg | |
| NM_001287246.1:c.3922G>A | NP_001274175.1:p.Gly1308Arg | |
| NM_001287247.1:c.3529G>A | NP_001274176.1:p.Gly1177Arg | |
| NM_001287248.1:c.2797G>A | NP_001274177.1:p.Gly933Arg | |
| XM_006720632.2:c.1960G>A | XP_006720695.1:p.Gly654Arg | |
| XM_011521881.1:c.2608G>A | XP_011520183.1:p.Gly870Arg | |
| XM_011521881.2:c.2608G>A | XP_011520183.1:p.Gly870Arg | |
| NM_000057.4:c.3922G>A MANE Select | NP_000048.1:p.Gly1308Arg | |
| NM_001287246.2:c.3922G>A | NP_001274175.1:p.Gly1308Arg | |
| NM_001287247.2:c.3529G>A | NP_001274176.1:p.Gly1177Arg | |
| NM_001287248.2:c.2797G>A | NP_001274177.1:p.Gly933Arg |