Canonical Allele Identifier: CA1697794744

Gene: CRHR2

Linked Data

• dbSNP Id: rs1784592785

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30678537G>C , CM000669.2:g.30678537G>C	GRCh38
NC_000007.13:g.30718153G>C , CM000669.1:g.30718153G>C	GRCh37
NC_000007.12:g.30684678G>C	NCBI36
NG_029169.1:g.26567C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000471646.6:c.229+3378C>G MANE Select	ENSP00000418722.1:n.229+3378C>G
ENST00000341843.8:c.187+3378C>G	ENSP00000344304.4:n.187+3378C>G
ENST00000348438.8:c.310+3378C>G	ENSP00000340943.4:n.310+3378C>G
ENST00000452278.5:c.*342+3378C>G	ENSP00000401930.1:n.*342+3378C>G
ENST00000471646.5:c.229+3378C>G	ENSP00000418722.1:n.229+3378C>G
ENST00000506074.6:c.229+3378C>G	ENSP00000426498.3:n.229+3378C>G
NM_001202475.1:c.310+3378C>G	NP_001189404.1:n.310+3378C>G
NM_001202481.1:c.187+3378C>G	NP_001189410.1:n.187+3378C>G
NM_001202482.1:c.229+3378C>G	NP_001189411.1:n.229+3378C>G
NM_001202483.1:c.229+3378C>G	NP_001189412.1:n.229+3378C>G
NM_001883.4:c.229+3378C>G	NP_001874.2:n.229+3378C>G
XM_011515127.1:c.229+3378C>G	XP_011513429.1:n.229+3378C>G
XM_011515128.1:c.229+3378C>G	XP_011513430.1:n.229+3378C>G
XM_011515129.1:c.229+3378C>G	XP_011513431.1:n.229+3378C>G
XM_017011752.2:c.187+3378C>G	XP_016867241.1:n.187+3378C>G
XM_024446665.1:c.229+3378C>G	XP_024302433.1:n.229+3378C>G
NM_001883.5:c.229+3378C>G MANE Select	NP_001874.2:n.229+3378C>G
NM_001202482.2:c.229+3378C>G	NP_001189411.1:n.229+3378C>G
NM_001202483.2:c.229+3378C>G	NP_001189412.1:n.229+3378C>G