Canonical Allele Identifier: CA1697794590

Gene: CRHR2

Linked Data

• dbSNP Id: rs1784587834

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30678379_30678380del , CM000669.2:g.30678379_30678380del	GRCh38
NC_000007.13:g.30717995_30717996del , CM000669.1:g.30717995_30717996del	GRCh37
NC_000007.12:g.30684520_30684521del	NCBI36
NG_029169.1:g.26724_26725del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471646.6:c.229+3535_229+3536del MANE Select	ENSP00000418722.1:n.229+3535_229+3536del
ENST00000341843.8:c.187+3535_187+3536del	ENSP00000344304.4:n.187+3535_187+3536del
ENST00000348438.8:c.310+3535_310+3536del	ENSP00000340943.4:n.310+3535_310+3536del
ENST00000452278.5:c.*342+3535_*342+3536del	ENSP00000401930.1:n.*342+3535_*342+3536del
ENST00000471646.5:c.229+3535_229+3536del	ENSP00000418722.1:n.229+3535_229+3536del
ENST00000506074.6:c.229+3535_229+3536del	ENSP00000426498.3:n.229+3535_229+3536del
NM_001202475.1:c.310+3535_310+3536del	NP_001189404.1:n.310+3535_310+3536del
NM_001202481.1:c.187+3535_187+3536del	NP_001189410.1:n.187+3535_187+3536del
NM_001202482.1:c.229+3535_229+3536del	NP_001189411.1:n.229+3535_229+3536del
NM_001202483.1:c.229+3535_229+3536del	NP_001189412.1:n.229+3535_229+3536del
NM_001883.4:c.229+3535_229+3536del	NP_001874.2:n.229+3535_229+3536del
XM_011515127.1:c.229+3535_229+3536del	XP_011513429.1:n.229+3535_229+3536del
XM_011515128.1:c.229+3535_229+3536del	XP_011513430.1:n.229+3535_229+3536del
XM_011515129.1:c.229+3535_229+3536del	XP_011513431.1:n.229+3535_229+3536del
XM_017011752.2:c.187+3535_187+3536del	XP_016867241.1:n.187+3535_187+3536del
XM_024446665.1:c.229+3535_229+3536del	XP_024302433.1:n.229+3535_229+3536del
NM_001883.5:c.229+3535_229+3536del MANE Select	NP_001874.2:n.229+3535_229+3536del
NM_001202482.2:c.229+3535_229+3536del	NP_001189411.1:n.229+3535_229+3536del
NM_001202483.2:c.229+3535_229+3536del	NP_001189412.1:n.229+3535_229+3536del