gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.97683336 (EAS)
Genomes Max Group AF
0.97683336 (EAS)
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.45818213C>T , CM000679.2:g.45818213C>T | GRCh38 |
| NC_000017.10:g.43895579C>T , CM000679.1:g.43895579C>T | GRCh37 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000580876.6:c.-285+1631C>T (CRHR1) | ENSP00000516345.1:n.-285+1631C>T | |
| ENST00000580955.6:n.144+1631C>T (CRHR1) | ||
| ENST00000705340.1:n.516+1291C>T (CRHR1) | ||
| ENST00000705341.1:c.524+1631C>T (CRHR1) | ENSP00000516114.1:n.524+1631C>T | |
| ENST00000705342.1:n.29+1631C>T (CRHR1) | ||
| ENST00000314537.10:c.241+1631C>T (CRHR1) MANE Select | ENSP00000326060.6:n.241+1631C>T | |
| ENST00000293493.11:c.241+1631C>T (CRHR1) | ENSP00000293493.8:n.241+1631C>T | |
| ENST00000314537.9:c.241+1631C>T (CRHR1) | ENSP00000326060.5:n.241+1631C>T | |
| ENST00000339069.9:c.24+1631C>T (CRHR1) | ENSP00000340522.6:n.24+1631C>T | |
| ENST00000347197.9:c.241+1631C>T (CRHR1) | ENSP00000239167.7:n.241+1631C>T | |
| ENST00000352855.9:c.122-3142C>T (CRHR1) | ENSP00000344068.5:n.122-3142C>T | |
| ENST00000398285.7:c.241+1631C>T (CRHR1) | ENSP00000381333.3:n.241+1631C>T | |
| ENST00000577353.5:c.241+1631C>T (CRHR1) | ENSP00000462016.1:n.241+1631C>T | |
| ENST00000580955.5:c.144+1631C>T (CRHR1) | ||
| ENST00000582766.5:n.98-3142C>T (CRHR1) | ||
| ENST00000583888.1:c.25+1631C>T (CRHR1) | ENSP00000462553.1:n.25+1631C>T | |
| ENST00000619154.4:c.122-11002C>T (CRHR1) | ENSP00000484545.1:n.122-11002C>T | |
| ENST00000634540.1:c.-285+1631C>T (LINC02210-CRHR1) | ENSP00000488912.1:n.-285+1631C>T | |
| NM_001145146.1:c.241+1631C>T (CRHR1) | NP_001138618.1:n.241+1631C>T | |
| NM_001145147.1:c.122-3142C>T (CRHR1) | NP_001138619.1:n.122-3142C>T | |
| NM_001145148.1:c.241+1631C>T (CRHR1) | NP_001138620.1:n.241+1631C>T | |
| NM_001256299.2:c.-285+1631C>T (LINC02210-CRHR1) | NP_001243228.1:n.-285+1631C>T | |
| NM_001303016.1:c.24+1631C>T (LINC02210-CRHR1) | NP_001289945.1:n.24+1631C>T | |
| NM_001303018.1:c.-198-11002C>T (CRHR1) | NP_001289947.1:n.-198-11002C>T | |
| NM_001303020.1:c.24+1631C>T (CRHR1) | NP_001289949.1:n.24+1631C>T | |
| NM_004382.4:c.241+1631C>T (CRHR1) | NP_004373.2:n.241+1631C>T | |
| NM_001145146.2:c.241+1631C>T (CRHR1) | NP_001138618.1:n.241+1631C>T | |
| NM_001145147.2:c.122-3142C>T (CRHR1) | NP_001138619.1:n.122-3142C>T | |
| NM_001145148.2:c.241+1631C>T (CRHR1) | NP_001138620.1:n.241+1631C>T | |
| NM_001256299.3:c.-285+1631C>T (LINC02210-CRHR1) | NP_001243228.1:n.-285+1631C>T | |
| NM_001303018.2:c.-198-11002C>T (CRHR1) | NP_001289947.1:n.-198-11002C>T | |
| NM_004382.5:c.241+1631C>T (CRHR1) MANE Select | NP_004373.2:n.241+1631C>T | |
| NM_001303020.2:c.24+1631C>T (CRHR1) | NP_001289949.1:n.24+1631C>T |