Canonical Allele Identifier: CA12492763
Gene: VIPR2 HGNC NCBI

Linked Data

dbSNP Id: rs2071625
gnomAD v2: 7-158825020-C-T
gnomAD v3: 7-159032329-C-T
gnomAD v4: 7-159032329-C-T
MyVariant Identifiers: chr7:g.158825020C>T (hg19) chr7:g.159032329C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.159032329C>T , CM000669.2:g.159032329C>T GRCh38
NC_000007.13:g.158825020C>T , CM000669.1:g.158825020C>T GRCh37
NC_000007.12:g.158517781C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000262178.7:c.972-262G>A MANE Select ENSP00000262178.2:n.972-262G>A
ENST00000262178.6:c.972-262G>A ENSP00000262178.2:n.972-262G>A
ENST00000377633.7:c.924-262G>A ENSP00000366860.3:n.924-262G>A
ENST00000402066.5:c.1395-262G>A ENSP00000384497.1:n.1395-262G>A
NM_001304522.1:c.732-262G>A NP_001291451.1:n.732-262G>A
NM_001308259.1:c.924-262G>A NP_001295188.1:n.924-262G>A
NM_003382.4:c.972-262G>A NP_003373.2:n.972-262G>A
NR_130758.1:n.1158-262G>A
XM_005249561.2:c.1047-262G>A XP_005249618.1:n.1047-262G>A
XM_006716107.1:c.972-262G>A XP_006716170.1:n.972-262G>A
XM_006716108.2:c.783-262G>A XP_006716171.1:n.783-262G>A
XM_011516550.1:c.924-262G>A XP_011514852.1:n.924-262G>A
XM_011516552.1:c.558-262G>A XP_011514854.1:n.558-262G>A
XM_005249561.3:c.1047-262G>A XP_005249618.1:n.1047-262G>A
XM_006716107.2:c.972-262G>A XP_006716170.1:n.972-262G>A
XM_006716108.3:c.783-262G>A XP_006716171.1:n.783-262G>A
XM_011516550.2:c.924-262G>A XP_011514852.1:n.924-262G>A
XM_017012580.1:c.558-262G>A XP_016868069.1:n.558-262G>A
XM_024446914.1:c.1047-262G>A XP_024302682.1:n.1047-262G>A
XM_024446915.1:c.1047-262G>A XP_024302683.1:n.1047-262G>A
XM_024446916.1:c.972-262G>A XP_024302684.1:n.972-262G>A
XM_024446917.1:c.783-262G>A XP_024302685.1:n.783-262G>A
XM_024446918.1:c.558-262G>A XP_024302686.1:n.558-262G>A
NM_003382.5:c.972-262G>A MANE Select NP_003373.2:n.972-262G>A
NM_001304522.2:c.732-262G>A NP_001291451.1:n.732-262G>A
NR_130758.2:n.1068-262G>A
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