Linked Data
dbSNP Id:
rs1245956459
gnomAD v2:
12-52452880-C-G
gnomAD v3:
12-52059096-C-G
gnomAD v4:
12-52059096-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52059096C>G , CM000674.2:g.52059096C>G | GRCh38 |
| NC_000012.11:g.52452880C>G , CM000674.1:g.52452880C>G | GRCh37 |
| NC_000012.10:g.50739147C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000394825.6:c.*152C>G (NR4A1) MANE Select | ENSP00000378302.1:n.*152C>G | |
| ENST00000243050.5:c.*152C>G (NR4A1) | ENSP00000243050.1:n.*152C>G | |
| ENST00000360284.7:c.*152C>G (NR4A1) | ENSP00000353427.3:n.*152C>G | |
| ENST00000394824.2:c.*152C>G (NR4A1) | ENSP00000378301.2:n.*152C>G | |
| ENST00000394825.5:c.*152C>G (NR4A1) | ENSP00000378302.1:n.*152C>G | |
| ENST00000545748.5:c.*152C>G (NR4A1) | ENSP00000440864.1:n.*152C>G | |
| ENST00000550557.1:n.4430C>G (NR4A1) | ||
| NM_001202233.1:c.*152C>G (NR4A1) | NP_001189162.1:n.*152C>G | |
| NM_001202234.1:c.*152C>G (NR4A1) | NP_001189163.1:n.*152C>G | |
| NM_002135.4:c.*152C>G (NR4A1) | NP_002126.2:n.*152C>G | |
| NM_173157.2:c.*152C>G (NR4A1) | NP_775180.1:n.*152C>G | |
| XM_005268822.3:c.*152C>G (NR4A1) | XP_005268879.1:n.*152C>G | |
| XM_005268824.2:c.*152C>G (NR4A1) | XP_005268881.1:n.*152C>G | |
| XM_006719363.1:c.*152C>G (NR4A1) | XP_006719426.1:n.*152C>G | |
| XM_006719364.2:c.*152C>G (NR4A1) | XP_006719427.1:n.*152C>G | |
| XM_011538250.1:c.*152C>G (NR4A1) | XP_011536552.1:n.*152C>G | |
| XM_005268824.3:c.*152C>G (NR4A1) | XP_005268881.1:n.*152C>G | |
| XM_006719364.4:c.*152C>G (NR4A1) | XP_006719427.1:n.*152C>G | |
| XM_017019247.1:c.*152C>G (NR4A1) | XP_016874736.1:n.*152C>G | |
| NM_173157.3:c.*152C>G (NR4A1) MANE Select | NP_775180.1:n.*152C>G | |
| NM_001202233.2:c.*152C>G (NR4A1) | NP_001189162.1:n.*152C>G | |
| NM_001202234.2:c.*152C>G (NR4A1) | NP_001189163.1:n.*152C>G | |
| NM_002135.5:c.*152C>G (NR4A1) | NP_002126.2:n.*152C>G | |
| NR_170321.1:n.400+5G>C (NR4A1AS) |