Linked Data
dbSNP Id:
rs1876828
gnomAD v2:
17-43911525-C-T
gnomAD v3:
17-45834159-C-T
gnomAD v4:
17-45834159-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.45834159C>T , CM000679.2:g.45834159C>T | GRCh38 |
| NC_000017.10:g.43911525C>T , CM000679.1:g.43911525C>T | GRCh37 |
| NC_000017.9:g.41267306C>T | NCBI36 |
| NG_009902.1:g.54898C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000580876.6:c.446+111C>T (CRHR1) | ENSP00000516345.1:n.446+111C>T | |
| ENST00000580955.6:n.1322+111C>T (CRHR1) | ||
| ENST00000705340.1:n.1382+111C>T (CRHR1) | ||
| ENST00000705341.1:c.*784+111C>T (CRHR1) | ENSP00000516114.1:n.*784+111C>T | |
| ENST00000705342.1:n.1364+111C>T (CRHR1) | ||
| ENST00000705343.1:n.1347+111C>T (CRHR1) | ||
| ENST00000705344.1:n.911+111C>T (CRHR1) | ||
| ENST00000705345.1:n.1289+111C>T (CRHR1) | ||
| ENST00000314537.10:c.1107+111C>T (CRHR1) MANE Select | ENSP00000326060.6:n.1107+111C>T | |
| ENST00000293493.11:c.1152+310C>T (CRHR1) | ENSP00000293493.8:n.1152+310C>T | |
| ENST00000314537.9:c.1107+111C>T (CRHR1) | ENSP00000326060.5:n.1107+111C>T | |
| ENST00000339069.9:c.804+111C>T (CRHR1) | ENSP00000340522.6:n.804+111C>T | |
| ENST00000347197.9:c.*584+111C>T (CRHR1) | ENSP00000239167.7:n.*584+111C>T | |
| ENST00000352855.9:c.987+111C>T (CRHR1) | ENSP00000344068.5:n.987+111C>T | |
| ENST00000398285.7:c.1194+111C>T (CRHR1) | ENSP00000381333.3:n.1194+111C>T | |
| ENST00000535778.2:c.251+111C>T (CRHR1) | ||
| ENST00000577353.5:c.1065+310C>T (CRHR1) | ENSP00000462016.1:n.1065+310C>T | |
| ENST00000580876.5:c.201+111C>T (CRHR1) | ||
| ENST00000583888.1:c.560-465C>T (CRHR1) | ENSP00000462553.1:n.560-465C>T | |
| ENST00000619154.4:c.*436+111C>T (CRHR1) | ENSP00000484545.1:n.*436+111C>T | |
| ENST00000634540.1:c.582+111C>T (LINC02210-CRHR1) | ENSP00000488912.1:n.582+111C>T | |
| NM_001145146.1:c.1194+111C>T (CRHR1) | NP_001138618.1:n.1194+111C>T | |
| NM_001145147.1:c.987+111C>T (CRHR1) | NP_001138619.1:n.987+111C>T | |
| NM_001145148.1:c.1065+310C>T (CRHR1) | NP_001138620.1:n.1065+310C>T | |
| NM_001256299.2:c.582+111C>T (LINC02210-CRHR1) | NP_001243228.1:n.582+111C>T | |
| NM_001303016.1:c.668+111C>T (LINC02210-CRHR1) | NP_001289945.1:n.668+111C>T | |
| NM_001303018.1:c.582+111C>T (CRHR1) | NP_001289947.1:n.582+111C>T | |
| NM_001303020.1:c.804+111C>T (CRHR1) | NP_001289949.1:n.804+111C>T | |
| NM_004382.4:c.1107+111C>T (CRHR1) | NP_004373.2:n.1107+111C>T | |
| NM_001145146.2:c.1194+111C>T (CRHR1) | NP_001138618.1:n.1194+111C>T | |
| NM_001145147.2:c.987+111C>T (CRHR1) | NP_001138619.1:n.987+111C>T | |
| NM_001145148.2:c.1065+310C>T (CRHR1) | NP_001138620.1:n.1065+310C>T | |
| NM_001256299.3:c.582+111C>T (LINC02210-CRHR1) | NP_001243228.1:n.582+111C>T | |
| NM_001303018.2:c.582+111C>T (CRHR1) | NP_001289947.1:n.582+111C>T | |
| NM_004382.5:c.1107+111C>T (CRHR1) MANE Select | NP_004373.2:n.1107+111C>T | |
| NM_001303020.2:c.804+111C>T (CRHR1) | NP_001289949.1:n.804+111C>T |