Canonical Allele Identifier: CA1756436956

Gene: VIPR2

Linked Data

• dbSNP Id: rs1853814455
• gnomAD v4: 7-159034657-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.159034657G>A , CM000669.2:g.159034657G>A	GRCh38
NC_000007.13:g.158827348G>A , CM000669.1:g.158827348G>A	GRCh37
NC_000007.12:g.158520109G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262178.7:c.810-7C>T MANE Select	ENSP00000262178.2:n.810-7C>T
ENST00000262178.6:c.810-7C>T	ENSP00000262178.2:n.810-7C>T
ENST00000377633.7:c.762-7C>T	ENSP00000366860.3:n.762-7C>T
ENST00000402066.5:c.1233-7C>T	ENSP00000384497.1:n.1233-7C>T
NM_001304522.1:c.570-7C>T	NP_001291451.1:n.570-7C>T
NM_001308259.1:c.762-7C>T	NP_001295188.1:n.762-7C>T
NM_003382.4:c.810-7C>T	NP_003373.2:n.810-7C>T
NR_130758.1:n.996-7C>T
XM_005249561.2:c.885-7C>T	XP_005249618.1:n.885-7C>T
XM_006716107.1:c.810-7C>T	XP_006716170.1:n.810-7C>T
XM_006716108.2:c.621-7C>T	XP_006716171.1:n.621-7C>T
XM_011516550.1:c.762-7C>T	XP_011514852.1:n.762-7C>T
XM_011516552.1:c.396-7C>T	XP_011514854.1:n.396-7C>T
XR_242047.2:n.1205-7C>T
XM_005249561.3:c.885-7C>T	XP_005249618.1:n.885-7C>T
XM_006716107.2:c.810-7C>T	XP_006716170.1:n.810-7C>T
XM_006716108.3:c.621-7C>T	XP_006716171.1:n.621-7C>T
XM_011516550.2:c.762-7C>T	XP_011514852.1:n.762-7C>T
XM_017012580.1:c.396-7C>T	XP_016868069.1:n.396-7C>T
XM_024446914.1:c.885-7C>T	XP_024302682.1:n.885-7C>T
XM_024446915.1:c.885-7C>T	XP_024302683.1:n.885-7C>T
XM_024446916.1:c.810-7C>T	XP_024302684.1:n.810-7C>T
XM_024446917.1:c.621-7C>T	XP_024302685.1:n.621-7C>T
XM_024446918.1:c.396-7C>T	XP_024302686.1:n.396-7C>T
NM_003382.5:c.810-7C>T MANE Select	NP_003373.2:n.810-7C>T
NM_001304522.2:c.570-7C>T	NP_001291451.1:n.570-7C>T
NR_130758.2:n.906-7C>T