Canonical Allele Identifier: CA156053025

Gene: CRHR2

Linked Data

• dbSNP Id: rs1040926137
• gnomAD v3: 7-30678559-C-T
• gnomAD v4: 7-30678559-C-T
• MyVariant Identifiers: chr7:g.30718175C>T (hg19) ; chr7:g.30678559C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30678559C>T , CM000669.2:g.30678559C>T	GRCh38
NC_000007.13:g.30718175C>T , CM000669.1:g.30718175C>T	GRCh37
NC_000007.12:g.30684700C>T	NCBI36
NG_029169.1:g.26545G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000471646.6:c.229+3356G>A MANE Select	ENSP00000418722.1:n.229+3356G>A
ENST00000341843.8:c.187+3356G>A	ENSP00000344304.4:n.187+3356G>A
ENST00000348438.8:c.310+3356G>A	ENSP00000340943.4:n.310+3356G>A
ENST00000452278.5:c.*342+3356G>A	ENSP00000401930.1:n.*342+3356G>A
ENST00000471646.5:c.229+3356G>A	ENSP00000418722.1:n.229+3356G>A
ENST00000506074.6:c.229+3356G>A	ENSP00000426498.3:n.229+3356G>A
NM_001202475.1:c.310+3356G>A	NP_001189404.1:n.310+3356G>A
NM_001202481.1:c.187+3356G>A	NP_001189410.1:n.187+3356G>A
NM_001202482.1:c.229+3356G>A	NP_001189411.1:n.229+3356G>A
NM_001202483.1:c.229+3356G>A	NP_001189412.1:n.229+3356G>A
NM_001883.4:c.229+3356G>A	NP_001874.2:n.229+3356G>A
XM_011515127.1:c.229+3356G>A	XP_011513429.1:n.229+3356G>A
XM_011515128.1:c.229+3356G>A	XP_011513430.1:n.229+3356G>A
XM_011515129.1:c.229+3356G>A	XP_011513431.1:n.229+3356G>A
XM_017011752.2:c.187+3356G>A	XP_016867241.1:n.187+3356G>A
XM_024446665.1:c.229+3356G>A	XP_024302433.1:n.229+3356G>A
NM_001883.5:c.229+3356G>A MANE Select	NP_001874.2:n.229+3356G>A
NM_001202482.2:c.229+3356G>A	NP_001189411.1:n.229+3356G>A
NM_001202483.2:c.229+3356G>A	NP_001189412.1:n.229+3356G>A