gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.97688766 (EAS)
Genomes Max Group AF
0.97688766 (EAS)
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.45821843A>G , CM000679.2:g.45821843A>G | GRCh38 |
| NC_000017.10:g.43899209A>G , CM000679.1:g.43899209A>G | GRCh37 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000580876.6:c.-199+403A>G (CRHR1) | ENSP00000516345.1:n.-199+403A>G | |
| ENST00000580955.6:n.230+403A>G (CRHR1) | ||
| ENST00000705340.1:n.602+403A>G (CRHR1) | ||
| ENST00000705341.1:c.*4+403A>G (CRHR1) | ENSP00000516114.1:n.*4+403A>G | |
| ENST00000705342.1:n.115+403A>G (CRHR1) | ||
| ENST00000314537.10:c.327+403A>G (CRHR1) MANE Select | ENSP00000326060.6:n.327+403A>G | |
| ENST00000293493.11:c.327+403A>G (CRHR1) | ENSP00000293493.8:n.327+403A>G | |
| ENST00000314537.9:c.327+403A>G (CRHR1) | ENSP00000326060.5:n.327+403A>G | |
| ENST00000339069.9:c.24+5261A>G (CRHR1) | ENSP00000340522.6:n.24+5261A>G | |
| ENST00000347197.9:c.327+403A>G (CRHR1) | ENSP00000239167.7:n.327+403A>G | |
| ENST00000352855.9:c.207+403A>G (CRHR1) | ENSP00000344068.5:n.207+403A>G | |
| ENST00000398285.7:c.327+403A>G (CRHR1) | ENSP00000381333.3:n.327+403A>G | |
| ENST00000577353.5:c.327+403A>G (CRHR1) | ENSP00000462016.1:n.327+403A>G | |
| ENST00000580955.5:c.230+403A>G (CRHR1) | ||
| ENST00000582766.5:n.183+403A>G (CRHR1) | ||
| ENST00000583888.1:c.111+403A>G (CRHR1) | ENSP00000462553.1:n.111+403A>G | |
| ENST00000619154.4:c.122-7372A>G (CRHR1) | ENSP00000484545.1:n.122-7372A>G | |
| ENST00000634540.1:c.-199+403A>G (LINC02210-CRHR1) | ENSP00000488912.1:n.-199+403A>G | |
| NM_001145146.1:c.327+403A>G (CRHR1) | NP_001138618.1:n.327+403A>G | |
| NM_001145147.1:c.207+403A>G (CRHR1) | NP_001138619.1:n.207+403A>G | |
| NM_001145148.1:c.327+403A>G (CRHR1) | NP_001138620.1:n.327+403A>G | |
| NM_001256299.2:c.-199+403A>G (LINC02210-CRHR1) | NP_001243228.1:n.-199+403A>G | |
| NM_001303016.1:c.24+5261A>G (LINC02210-CRHR1) | NP_001289945.1:n.24+5261A>G | |
| NM_001303018.1:c.-198-7372A>G (CRHR1) | NP_001289947.1:n.-198-7372A>G | |
| NM_001303020.1:c.24+5261A>G (CRHR1) | NP_001289949.1:n.24+5261A>G | |
| NM_004382.4:c.327+403A>G (CRHR1) | NP_004373.2:n.327+403A>G | |
| NM_001145146.2:c.327+403A>G (CRHR1) | NP_001138618.1:n.327+403A>G | |
| NM_001145147.2:c.207+403A>G (CRHR1) | NP_001138619.1:n.207+403A>G | |
| NM_001145148.2:c.327+403A>G (CRHR1) | NP_001138620.1:n.327+403A>G | |
| NM_001256299.3:c.-199+403A>G (LINC02210-CRHR1) | NP_001243228.1:n.-199+403A>G | |
| NM_001303018.2:c.-198-7372A>G (CRHR1) | NP_001289947.1:n.-198-7372A>G | |
| NM_004382.5:c.327+403A>G (CRHR1) MANE Select | NP_004373.2:n.327+403A>G | |
| NM_001303020.2:c.24+5261A>G (CRHR1) | NP_001289949.1:n.24+5261A>G |