Canonical Allele Identifier: CA4206764
Gene: CRHR2 HGNC NCBI
COSMIC:
COSM5021539 (not active)
MyVariant.info:
GRCh38 chr7:g.30689292A>T
GRCh37 chr7:g.30728908A>T
gnomAD v2:
7:30728908 A / T
gnomAD v3:
7:30689292 A / T
gnomAD v4:
chr7-30689292-A-T
Joint Max Group AF 0.61113052 (NFE)
Genomes Max Group AF 0.60072118 (NFE)
Exomes Max Group AF 0.61151529 (NFE)
dbSNP:
255100
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30689292A>T , CM000669.2:g.30689292A>T GRCh38
NC_000007.13:g.30728908A>T , CM000669.1:g.30728908A>T GRCh37
NC_000007.12:g.30695433A>T NCBI36
NG_029169.1:g.15812T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000341843.8:c.-260-8T>A ENSP00000344304.4:n.-260-8T>A
ENST00000348438.8:c.91-8T>A ENSP00000340943.4:n.91-8T>A
ENST00000423776.1:c.91-8T>A ENSP00000416620.1:n.91-8T>A
ENST00000445981.5:c.91-8T>A ENSP00000401241.1:n.91-8T>A
ENST00000452278.5:c.91-8T>A ENSP00000401930.1:n.91-8T>A
ENST00000462882.1:n.187-8T>A
NM_001202475.1:c.91-8T>A NP_001189404.1:n.91-8T>A
NM_001202481.1:c.-260-8T>A NP_001189410.1:n.-260-8T>A
Search 100 bp 5'
Search 100 bp 3'