Canonical Allele Identifier: CA12502213
Gene: CRHR2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2284220

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30678487G>A , CM000669.2:g.30678487G>A GRCh38
NC_000007.13:g.30718103G>A , CM000669.1:g.30718103G>A GRCh37
NC_000007.12:g.30684628G>A NCBI36
NG_029169.1:g.26617C>T

Transcript Alleles

HGVS Amino-acid change
NM_001202475.1:c.310+3428C>T VV NP_001189404.1:p.=
NM_001202481.1:c.187+3428C>T VV NP_001189410.1:p.=
NM_001202482.1:c.229+3428C>T VV NP_001189411.1:p.=
NM_001202483.1:c.229+3428C>T VV NP_001189412.1:p.=
NM_001883.4:c.229+3428C>T VV NP_001874.2:p.=
XM_011515127.1:c.229+3428C>T XP_011513429.1:p.=
XM_011515128.1:c.229+3428C>T XP_011513430.1:p.=
XM_011515129.1:c.229+3428C>T XP_011513431.1:p.=
XM_017011752.2:c.187+3428C>T XP_016867241.1:p.=
XM_024446665.1:c.229+3428C>T XP_024302433.1:p.=
NM_001883.5:c.229+3428C>T VV MANE Preferred NP_001874.2:p.=
ENST00000341843.8:c.187+3428C>T ENSP00000344304.4:p.=
ENST00000348438.8:c.310+3428C>T ENSP00000340943.4:p.=
ENST00000452278.5:c.*342+3428C>T ENSP00000401930.1:p.=
ENST00000471646.5:c.229+3428C>T ENSP00000418722.1:p.=
ENST00000506074.6:c.229+3428C>T ENSP00000426498.3:p.=