Canonical Allele Identifier: CA1697794549
Gene: CRHR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30678339G= , CM000669.2:g.30678339G= GRCh38
NC_000007.13:g.30717955G= , CM000669.1:g.30717955G= GRCh37
NC_000007.12:g.30684480G= NCBI36
NG_029169.1:g.26765C=

Transcript Alleles

HGVS Amino-acid change
ENST00000471646.6:c.229+3576C= MANE Select ENSP00000418722.1:n.229+3576C=
ENST00000341843.8:c.187+3576C= ENSP00000344304.4:n.187+3576C=
ENST00000348438.8:c.310+3576C= ENSP00000340943.4:n.310+3576C=
ENST00000452278.5:c.*342+3576C= ENSP00000401930.1:n.*342+3576C=
ENST00000471646.5:c.229+3576C= ENSP00000418722.1:n.229+3576C=
ENST00000506074.6:c.229+3576C= ENSP00000426498.3:n.229+3576C=
NM_001202475.1:c.310+3576C= NP_001189404.1:n.310+3576C=
NM_001202481.1:c.187+3576C= NP_001189410.1:n.187+3576C=
NM_001202482.1:c.229+3576C= NP_001189411.1:n.229+3576C=
NM_001202483.1:c.229+3576C= NP_001189412.1:n.229+3576C=
NM_001883.4:c.229+3576C= NP_001874.2:n.229+3576C=
XM_011515127.1:c.229+3576C= XP_011513429.1:n.229+3576C=
XM_011515128.1:c.229+3576C= XP_011513430.1:n.229+3576C=
XM_011515129.1:c.229+3576C= XP_011513431.1:n.229+3576C=
XM_017011752.2:c.187+3576C= XP_016867241.1:n.187+3576C=
XM_024446665.1:c.229+3576C= XP_024302433.1:n.229+3576C=
NM_001883.5:c.229+3576C= MANE Select NP_001874.2:n.229+3576C=
NM_001202482.2:c.229+3576C= NP_001189411.1:n.229+3576C=
NM_001202483.2:c.229+3576C= NP_001189412.1:n.229+3576C=