Canonical Allele Identifier: CA369941619

Gene: VIPR2

Linked Data

• dbSNP Id: rs1222089056
• gnomAD v3: 7-159034647-G-C
• gnomAD v4: 7-159034647-G-C
• MyVariant Identifiers: chr7:g.158827338G>C (hg19) ; chr7:g.159034647G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.159034647G>C , CM000669.2:g.159034647G>C	GRCh38
NC_000007.13:g.158827338G>C , CM000669.1:g.158827338G>C	GRCh37
NC_000007.12:g.158520099G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262178.7:c.813C>G MANE Select	ENSP00000262178.2:p.Cys271Trp
ENST00000262178.6:c.813C>G	ENSP00000262178.2:p.Cys271Trp
ENST00000377633.7:c.765C>G	ENSP00000366860.3:p.Cys255Trp
ENST00000402066.5:c.1236C>G	ENSP00000384497.1:p.Cys412Trp
NM_001304522.1:c.573C>G	NP_001291451.1:p.Cys191Trp
NM_001308259.1:c.765C>G	NP_001295188.1:p.Cys255Trp
NM_003382.4:c.813C>G	NP_003373.2:p.Cys271Trp
NR_130758.1:n.999C>G
XM_005249561.2:c.888C>G	XP_005249618.1:p.Cys296Trp
XM_006716107.1:c.813C>G	XP_006716170.1:p.Cys271Trp
XM_006716108.2:c.624C>G	XP_006716171.1:p.Cys208Trp
XM_011516550.1:c.765C>G	XP_011514852.1:p.Cys255Trp
XM_011516552.1:c.399C>G	XP_011514854.1:p.Cys133Trp
XR_242047.2:n.1208C>G
XM_005249561.3:c.888C>G	XP_005249618.1:p.Cys296Trp
XM_006716107.2:c.813C>G	XP_006716170.1:p.Cys271Trp
XM_006716108.3:c.624C>G	XP_006716171.1:p.Cys208Trp
XM_011516550.2:c.765C>G	XP_011514852.1:p.Cys255Trp
XM_017012580.1:c.399C>G	XP_016868069.1:p.Cys133Trp
XM_024446914.1:c.888C>G	XP_024302682.1:p.Cys296Trp
XM_024446915.1:c.888C>G	XP_024302683.1:p.Cys296Trp
XM_024446916.1:c.813C>G	XP_024302684.1:p.Cys271Trp
XM_024446917.1:c.624C>G	XP_024302685.1:p.Cys208Trp
XM_024446918.1:c.399C>G	XP_024302686.1:p.Cys133Trp
NM_003382.5:c.813C>G MANE Select	NP_003373.2:p.Cys271Trp
NM_001304522.2:c.573C>G	NP_001291451.1:p.Cys191Trp
NR_130758.2:n.909C>G