Linked Data
dbSNP Id:
rs148994335
ExAC:
22:46748174 G / A
gnomAD v2:
22-46748174-G-A
gnomAD v3:
22-46352277-G-A
gnomAD v4:
22-46352277-G-A
COSMIC:
COSM285975
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.46352277G>A , CM000684.2:g.46352277G>A | GRCh38 |
| NC_000022.10:g.46748174G>A , CM000684.1:g.46748174G>A | GRCh37 |
| NC_000022.9:g.45126838G>A | NCBI36 |
| NG_012173.1:g.21877G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000465378.6:n.767G>A | ||
| ENST00000642923.1:c.614G>A | ENSP00000494255.1:p.Arg205Gln | |
| ENST00000643137.1:c.614G>A | ENSP00000495331.1:p.Arg205Gln | |
| ENST00000644006.1:c.*163G>A | ENSP00000493778.1:n.*163G>A | |
| ENST00000645026.1:n.770G>A | ||
| ENST00000645190.1:c.719G>A MANE Select | ENSP00000496496.1:p.Arg240Gln | |
| ENST00000647301.1:c.*163G>A | ENSP00000496641.1:n.*163G>A | |
| ENST00000290846.8:c.719G>A | ENSP00000290846.4:p.Arg240Gln | |
| ENST00000381019.3:c.719G>A | ENSP00000370407.3:p.Arg240Gln | |
| ENST00000381021.7:c.*312G>A | ENSP00000370409.3:n.*312G>A | |
| ENST00000441818.5:c.*253G>A | ENSP00000393014.1:n.*253G>A | |
| ENST00000453630.5:c.*257G>A | ENSP00000398488.1:n.*257G>A | |
| ENST00000456595.5:c.*253G>A | ENSP00000413880.1:n.*253G>A | |
| ENST00000457572.5:c.*163G>A | ENSP00000407700.1:n.*163G>A | |
| ENST00000463785.1:n.187G>A | ||
| ENST00000479648.1:n.539G>A | ||
| ENST00000485175.5:n.679G>A | ||
| ENST00000486620.5:n.761G>A | ||
| NM_001282782.1:c.377G>A | NP_001269711.1:p.Arg126Gln | |
| NM_001282783.1:c.299G>A | NP_001269712.1:p.Arg100Gln | |
| NM_001282784.1:c.299G>A | NP_001269713.1:p.Arg100Gln | |
| NM_001282785.1:c.719G>A | NP_001269714.1:p.Arg240Gln | |
| NM_018006.4:c.719G>A | NP_060476.2:p.Arg240Gln | |
| NR_104240.1:n.1028G>A | ||
| NR_104241.1:n.921G>A | ||
| XM_005261678.1:c.323G>A | XP_005261735.1:p.Arg108Gln | |
| XM_005261681.1:c.323G>A | XP_005261738.1:p.Arg108Gln | |
| XM_011530271.1:c.614G>A | XP_011528573.1:p.Arg205Gln | |
| XM_011530272.1:c.719G>A | XP_011528574.1:p.Arg240Gln | |
| XM_011530273.1:c.719G>A | XP_011528575.1:p.Arg240Gln | |
| XM_011530274.1:c.377G>A | XP_011528576.1:p.Arg126Gln | |
| XM_011530275.1:c.323G>A | XP_011528577.1:p.Arg108Gln | |
| XM_011530271.2:c.614G>A | XP_011528573.1:p.Arg205Gln | |
| XM_011530272.2:c.719G>A | XP_011528574.1:p.Arg240Gln | |
| XM_011530273.2:c.719G>A | XP_011528575.1:p.Arg240Gln | |
| XM_011530274.2:c.377G>A | XP_011528576.1:p.Arg126Gln | |
| XM_024452260.1:c.614G>A | XP_024308028.1:p.Arg205Gln | |
| XR_001755261.2:n.765G>A | ||
| XR_001755262.2:n.765G>A | ||
| NM_018006.5:c.719G>A MANE Select | NP_060476.2:p.Arg240Gln | |
| NM_001282782.2:c.377G>A | NP_001269711.1:p.Arg126Gln | |
| NM_001282783.2:c.299G>A | NP_001269712.1:p.Arg100Gln | |
| NM_001282784.2:c.299G>A | NP_001269713.1:p.Arg100Gln | |
| NM_001282785.2:c.719G>A | NP_001269714.1:p.Arg240Gln | |
| NR_104240.2:n.715G>A | ||
| NR_104241.2:n.608G>A |