Linked Data
dbSNP Id:
rs778251548
ExAC:
19:1388859 A / G
gnomAD v2:
19-1388859-A-G
gnomAD v3:
19-1388860-A-G
gnomAD v4:
19-1388860-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.1388860A>G , CM000681.2:g.1388860A>G | GRCh38 |
| NC_000019.9:g.1388859A>G , CM000681.1:g.1388859A>G | GRCh37 |
| NC_000019.8:g.1339859A>G | NCBI36 |
| NG_008283.1:g.9977A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000233627.14:c.150A>G MANE Select | ENSP00000233627.9:p.Arg50= | |
| ENST00000233627.13:c.150A>G | ENSP00000233627.9:p.Arg50= | |
| ENST00000313408.11:c.150A>G | ENSP00000364262.5:p.Arg50= | |
| ENST00000414651.3:c.240A>G | ENSP00000406630.2:p.Arg80= | |
| ENST00000436115.6:n.173A>G | ||
| ENST00000534853.5:c.145A>G | ENSP00000442822.1:p.Ser49Gly | |
| ENST00000535382.1:n.402A>G | ||
| ENST00000538523.5:n.206A>G | ||
| ENST00000538662.5:n.177A>G | ||
| ENST00000538929.5:n.240A>G | ||
| ENST00000539480.5:c.150A>G | ENSP00000443273.1:p.Arg50= | |
| ENST00000540530.5:n.141A>G | ||
| ENST00000543289.5:n.640A>G | ||
| ENST00000545446.5:n.441A>G | ||
| ENST00000546172.7:c.*146A>G | ENSP00000467094.1:n.*146A>G | |
| ENST00000546283.5:c.150A>G | ENSP00000440348.1:p.Arg50= | |
| ENST00000618074.4:c.150A>G | ENSP00000477895.1:p.Arg50= | |
| ENST00000620479.4:c.150A>G | ENSP00000480984.1:p.Arg50= | |
| ENST00000622587.4:n.146A>G | ||
| NM_024407.4:c.150A>G | NP_077718.3:p.Arg50= | |
| XM_005259556.3:c.150A>G | XP_005259613.2:p.Arg50= | |
| NM_001363602.1:c.150A>G | NP_001350531.1:p.Arg50= | |
| XM_017026768.2:c.150A>G | XP_016882257.2:p.Arg50= | |
| XM_024451499.1:c.171A>G | XP_024307267.1:p.Arg57= | |
| NM_024407.5:c.150A>G MANE Select | NP_077718.3:p.Arg50= | |
| NM_001363602.2:c.150A>G | NP_001350531.1:p.Arg50= |