Canonical Allele Identifier: CA837511315
Gene: CRHR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30687161A>C , CM000669.2:g.30687161A>C GRCh38
NC_000007.13:g.30726777A>C , CM000669.1:g.30726777A>C GRCh37
NC_000007.12:g.30693302A>C NCBI36
NG_029169.1:g.17943T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000341843.8:c.-166-546T>G ENSP00000344304.4:n.-166-546T>G
ENST00000348438.8:c.184+2030T>G ENSP00000340943.4:n.184+2030T>G
ENST00000423776.1:c.185-546T>G ENSP00000416620.1:n.185-546T>G
ENST00000445981.5:c.184+2030T>G ENSP00000401241.1:n.184+2030T>G
ENST00000452278.5:c.185-546T>G ENSP00000401930.1:n.185-546T>G
ENST00000462882.1:n.476-546T>G
NM_001202475.1:c.184+2030T>G NP_001189404.1:n.184+2030T>G
NM_001202481.1:c.-166-546T>G NP_001189410.1:n.-166-546T>G
XM_017011752.2:c.-712T>G XP_016867241.1:n.-712T>G
XM_024446665.1:c.-825T>G XP_024302433.1:n.-825T>G