Canonical Allele Identifier: CA12552817
Gene: VIPR2 HGNC NCBI
MyVariant.info:
GRCh38 chr7:g.159028856G>A
GRCh37 chr7:g.158821547G>A
gnomAD v2:
7:158821547 G / A
gnomAD v3:
7:159028856 G / A
gnomAD v4:
chr7-159028856-G-A
Joint Max Group AF 0.57022869 (NFE)
Genomes Max Group AF 0.57034397 (NFE)
Exomes Max Group AF 0.43497213 (NFE)
dbSNP:
885861
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.159028856G>A , CM000669.2:g.159028856G>A GRCh38
NC_000007.13:g.158821547G>A , CM000669.1:g.158821547G>A GRCh37
NC_000007.12:g.158514308G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000262178.7:c.*1760C>T MANE Select ENSP00000262178.2:n.*1760C>T
ENST00000262178.6:c.*1760C>T ENSP00000262178.2:n.*1760C>T
NM_001304522.1:c.*1760C>T NP_001291451.1:n.*1760C>T
NM_001308259.1:c.*1760C>T NP_001295188.1:n.*1760C>T
NM_003382.4:c.*1760C>T NP_003373.2:n.*1760C>T
NR_130758.1:n.3597C>T
XM_005249561.3:c.*1760C>T XP_005249618.1:n.*1760C>T
XM_017012580.1:c.*1760C>T XP_016868069.1:n.*1760C>T
XM_024446914.1:c.*1760C>T XP_024302682.1:n.*1760C>T
XM_024446915.1:c.*1760C>T XP_024302683.1:n.*1760C>T
XM_024446916.1:c.*1760C>T XP_024302684.1:n.*1760C>T
XM_024446917.1:c.*1760C>T XP_024302685.1:n.*1760C>T
XM_024446918.1:c.*1760C>T XP_024302686.1:n.*1760C>T
NM_003382.5:c.*1760C>T MANE Select NP_003373.2:n.*1760C>T
NM_001304522.2:c.*1760C>T NP_001291451.1:n.*1760C>T
NR_130758.2:n.3507C>T
Search 100 bp 5'
Search 100 bp 3'