Canonical Allele Identifier: CA8616736
Gene: CRHR1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs16940665

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.45830530T>C , CM000679.2:g.45830530T>C GRCh38
NC_000017.10:g.43907896T>C , CM000679.1:g.43907896T>C GRCh37
NC_000017.9:g.41263677T>C NCBI36
NG_009902.1:g.51269T>C

Transcript Alleles

HGVS Amino-acid change
NM_001145146.1:c.756T>C VV NP_001138618.1:p.Thr252=
NM_001145147.1:c.549T>C VV NP_001138619.1:p.Thr183=
NM_001145148.1:c.669T>C VV NP_001138620.1:p.Thr223=
NM_001256299.2:c.144T>C VV NP_001243228.1:p.Thr48=
NM_001303016.1:c.366T>C VV NP_001289945.1:p.Thr122=
NM_001303018.1:c.144T>C VV NP_001289947.1:p.Thr48=
NM_001303020.1:c.366T>C VV NP_001289949.1:p.Thr122=
NM_004382.4:c.669T>C VV NP_004373.2:p.Thr223=
ENST00000293493.11:c.756T>C ENSP00000293493.8:p.Thr252=
ENST00000314537.9:c.669T>C ENSP00000326060.5:p.Thr223=
ENST00000339069.9:c.366T>C ENSP00000340522.6:p.Thr122=
ENST00000347197.9:c.*146T>C ENSP00000239167.7:p.=
ENST00000352855.9:c.549T>C ENSP00000344068.5:p.Thr183=
ENST00000398285.7:n.756T>C ENSP00000381333.3:p.Thr252=
ENST00000577353.5:n.669T>C ENSP00000462016.1:p.Thr223=
ENST00000581479.1:n.131T>C
ENST00000582766.5:n.727T>C
ENST00000583888.1:n.339+316T>C ENSP00000462553.1:p.=
ENST00000619154.4:c.463T>C ENSP00000484545.1:p.Ter155Arg
ENST00000634540.1:c.144T>C ENSP00000488912.1:p.Thr48=