Linked Data
ClinVar Variation Id:
459963
dbSNP Id:
rs746598421
ExAC:
4:159627469 G / A
gnomAD v2:
4-159627469-G-A
gnomAD v4:
4-158706317-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.158706317G>A , CM000666.2:g.158706317G>A | GRCh38 |
| NC_000004.11:g.159627469G>A , CM000666.1:g.159627469G>A | GRCh37 |
| NC_000004.10:g.159846919G>A | NCBI36 |
| NG_007078.2:g.38976G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000681978.1:n.2950G>A | ||
| ENST00000682178.1:n.2446G>A | ||
| ENST00000682345.1:c.*1114G>A | ENSP00000508122.1:n.*1114G>A | |
| ENST00000682452.1:n.1745G>A | ||
| ENST00000682456.1:c.1273G>A | ENSP00000508240.1:p.Gly425Arg | |
| ENST00000682566.1:n.2197G>A | ||
| ENST00000682613.1:n.1726G>A | ||
| ENST00000682734.1:c.241G>A | ENSP00000507860.1:p.Gly81Arg | |
| ENST00000682820.1:n.1451G>A | ||
| ENST00000683004.1:c.*1107G>A | ENSP00000506936.1:n.*1107G>A | |
| ENST00000683079.1:c.*839G>A | ENSP00000507296.1:n.*839G>A | |
| ENST00000683081.1:c.*1251G>A | ENSP00000507722.1:n.*1251G>A | |
| ENST00000683181.1:n.693G>A | ||
| ENST00000683209.1:n.3740G>A | ||
| ENST00000683305.1:c.1231G>A | ENSP00000508043.1:p.Gly411Arg | |
| ENST00000683448.1:c.*334G>A | ENSP00000506931.1:n.*334G>A | |
| ENST00000683478.1:c.*765G>A | ENSP00000507793.1:n.*765G>A | |
| ENST00000683483.1:c.1270G>A | ENSP00000507719.1:p.Gly424Arg | |
| ENST00000683622.1:n.1128G>A | ||
| ENST00000683751.1:c.919G>A | ENSP00000506944.1:p.Gly307Arg | |
| ENST00000684036.1:c.1231G>A | ENSP00000507276.1:p.Gly411Arg | |
| ENST00000684129.1:c.241G>A | ENSP00000507174.1:p.Gly81Arg | |
| ENST00000684209.1:n.1789G>A | ||
| ENST00000684296.1:c.*334G>A | ENSP00000507740.1:n.*334G>A | |
| ENST00000684505.1:c.1363G>A | ENSP00000508237.1:p.Gly455Arg | |
| ENST00000684552.1:c.*2833G>A | ENSP00000506899.1:n.*2833G>A | |
| ENST00000684611.1:n.3142G>A | ||
| ENST00000684622.1:c.1414G>A | ENSP00000507546.1:p.Gly472Arg | |
| ENST00000684627.1:c.1231G>A | ENSP00000507471.1:p.Gly411Arg | |
| ENST00000684641.1:c.1129G>A | ENSP00000507642.1:p.Gly377Arg | |
| ENST00000684675.1:c.*261G>A | ENSP00000506934.1:n.*261G>A | |
| ENST00000684749.1:n.1483G>A | ||
| ENST00000511912.6:c.1414G>A MANE Select | ENSP00000426638.1:p.Gly472Arg | |
| ENST00000307738.5:c.1273G>A | ENSP00000303552.5:p.Gly425Arg | |
| ENST00000506422.1:n.384G>A | ||
| ENST00000511912.5:c.1414G>A | ENSP00000426638.1:p.Gly472Arg | |
| NM_001281737.1:c.1273G>A | NP_001268666.1:p.Gly425Arg | |
| NM_001281738.1:c.1231G>A | NP_001268667.1:p.Gly411Arg | |
| NM_004453.3:c.1414G>A | NP_004444.2:p.Gly472Arg | |
| XM_024453935.1:c.1231G>A | XP_024309703.1:p.Gly411Arg | |
| NM_004453.4:c.1414G>A MANE Select | NP_004444.2:p.Gly472Arg | |
| NM_001281737.2:c.1273G>A | NP_001268666.1:p.Gly425Arg |