Linked Data
dbSNP Id:
rs1169217714
gnomAD v2:
5-53247423-A-G
gnomAD v3:
5-53951593-A-G
gnomAD v4:
5-53951593-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.53951593A>G , CM000667.2:g.53951593A>G | GRCh38 |
| NC_000005.9:g.53247423A>G , CM000667.1:g.53247423A>G | GRCh37 |
| NC_000005.8:g.53283180A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000504924.6:c.463-64880T>C (ARL15) MANE Select | ENSP00000433427.1:n.463-64880T>C | |
| ENST00000502271.5:c.-75-64880T>C (ARL15) | ENSP00000473508.1:n.-75-64880T>C | |
| ENST00000504924.5:c.463-64880T>C (ARL15) | ENSP00000433427.1:n.463-64880T>C | |
| ENST00000507646.2:c.463-64210T>C (ARL15) | ENSP00000432680.1:n.463-64210T>C | |
| ENST00000510591.6:n.536-64880T>C (ARL15) | ||
| ENST00000620747.4:c.469-64886T>C (ARL15) | ENSP00000478984.1:n.469-64886T>C | |
| NM_019087.2:c.463-64880T>C (ARL15) | NP_061960.1:n.463-64880T>C | |
| NR_030307.1:n.7T>C (MIR581) | ||
| XM_011543498.1:c.646-64880T>C (ARL15) | XP_011541800.1:n.646-64880T>C | |
| XM_011543499.1:c.589-64880T>C (ARL15) | XP_011541801.1:n.589-64880T>C | |
| XM_011543500.1:c.520-64880T>C (ARL15) | XP_011541802.1:n.520-64880T>C | |
| XM_011543498.2:c.646-64880T>C (ARL15) | XP_011541800.1:n.646-64880T>C | |
| XM_011543499.2:c.589-64880T>C (ARL15) | XP_011541801.1:n.589-64880T>C | |
| XM_011543500.2:c.520-64880T>C (ARL15) | XP_011541802.1:n.520-64880T>C | |
| XM_017009598.1:c.469-64880T>C (ARL15) | XP_016865087.1:n.469-64880T>C | |
| NM_019087.3:c.463-64880T>C (ARL15) MANE Select | NP_061960.1:n.463-64880T>C |