Linked Data
dbSNP Id:
rs564863300
ExAC:
20:3897587 A / G
gnomAD v2:
20-3897587-A-G
gnomAD v3:
20-3916940-A-G
gnomAD v4:
20-3916940-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.3916940A>G , CM000682.2:g.3916940A>G | GRCh38 |
| NC_000020.10:g.3897587A>G , CM000682.1:g.3897587A>G | GRCh37 |
| NC_000020.9:g.3845587A>G | NCBI36 |
| NG_008131.3:g.33102A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000610179.7:c.1096A>G MANE Select | ENSP00000477429.2:p.Met366Val | |
| ENST00000316562.9:c.1426A>G | ENSP00000313377.4:p.Met476Val | |
| ENST00000336066.8:c.*437A>G | ENSP00000477229.2:n.*437A>G | |
| ENST00000610179.6:c.1096A>G | ENSP00000477429.2:p.Met366Val | |
| ENST00000643504.2:c.*726A>G | ENSP00000495157.2:n.*726A>G | |
| ENST00000646394.1:c.923A>G | ||
| ENST00000316562.8:c.1426A>G | ENSP00000313377.4:p.Met476Val | |
| ENST00000336066.7:c.*437A>G | ENSP00000477229.1:n.*437A>G | |
| ENST00000464452.1:n.661A>G | ||
| ENST00000495692.5:c.118A>G | ENSP00000476745.1:p.Met40Val | |
| ENST00000497424.5:c.553A>G | ENSP00000417609.1:p.Met185Val | |
| ENST00000610179.5:c.1057A>G | ENSP00000477429.1:p.Met353Val | |
| ENST00000621507.1:c.553A>G | ENSP00000481523.1:p.Met185Val | |
| NM_024960.4:c.553A>G | NP_079236.3:p.Met185Val | |
| NM_153638.2:c.1426A>G | NP_705902.2:p.Met476Val | |
| NM_153640.2:c.553A>G | NP_705904.1:p.Met185Val | |
| XM_005260835.2:c.811A>G | XP_005260892.1:p.Met271Val | |
| XM_005260836.3:c.553A>G | XP_005260893.3:p.Met185Val | |
| XM_006723631.1:c.553A>G | XP_006723694.1:p.Met185Val | |
| XM_011529364.1:c.1249A>G | XP_011527666.1:p.Met417Val | |
| NM_001324191.1:c.553A>G | NP_001311120.1:p.Met185Val | |
| NM_001324193.1:c.118A>G | NP_001311122.1:p.Met40Val | |
| NM_024960.5:c.553A>G | NP_079236.3:p.Met185Val | |
| NM_153638.3:c.1426A>G | NP_705902.2:p.Met476Val | |
| NM_153640.3:c.553A>G | NP_705904.1:p.Met185Val | |
| NR_136715.1:n.1450A>G | ||
| XM_005260835.3:c.811A>G | XP_005260892.1:p.Met271Val | |
| XM_005260836.4:c.553A>G | XP_005260893.3:p.Met185Val | |
| XM_011529364.3:c.1249A>G | XP_011527666.1:p.Met417Val | |
| XM_017028077.2:c.118A>G | XP_016883566.1:p.Met40Val | |
| XM_017028078.2:c.118A>G | XP_016883567.1:p.Met40Val | |
| XM_017028079.2:c.118A>G | XP_016883568.1:p.Met40Val | |
| XM_024452002.1:c.118A>G | XP_024307770.1:p.Met40Val | |
| XR_002958533.1:n.2214A>G | ||
| NM_001324191.2:c.553A>G | NP_001311120.1:p.Met185Val | |
| NM_001324193.2:c.118A>G | NP_001311122.1:p.Met40Val | |
| NM_024960.6:c.553A>G | NP_079236.3:p.Met185Val | |
| NR_136715.2:n.997A>G | ||
| NM_001386393.1:c.1096A>G MANE Select | NP_001373322.1:p.Met366Val | |
| NM_153638.4:c.1426A>G | NP_705902.2:p.Met476Val | |
| NM_153640.4:c.553A>G | NP_705904.1:p.Met185Val |