Canonical Allele Identifier: CA1069773490

Gene: NPY2R

Linked Data

• dbSNP Id: rs867193620
• gnomAD v3: 4-155209776-G-A
• gnomAD v4: 4-155209776-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.155209776G>A , CM000666.2:g.155209776G>A	GRCh38
NC_000004.11:g.156130928G>A , CM000666.1:g.156130928G>A	GRCh37
NC_000004.10:g.156350378G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329476.4:c.-49+707G>A MANE Select	ENSP00000332591.3:n.-49+707G>A
ENST00000329476.3:c.-49+707G>A	ENSP00000332591.3:n.-49+707G>A
ENST00000506608.1:c.-49+711G>A	ENSP00000426366.1:n.-49+711G>A
NM_000910.3:c.-49+707G>A	NP_000901.1:n.-49+707G>A
XM_005263033.3:c.-48-4116G>A	XP_005263090.1:n.-48-4116G>A
XM_005263034.3:c.-49+711G>A	XP_005263091.1:n.-49+711G>A
XM_005263033.4:c.-48-4116G>A	XP_005263090.1:n.-48-4116G>A
XM_005263034.4:c.-49+711G>A	XP_005263091.1:n.-49+711G>A
NM_000910.4:c.-49+707G>A MANE Select	NP_000901.1:n.-49+707G>A
NM_001370180.1:c.-49+711G>A	NP_001357109.1:n.-49+711G>A
NM_001375470.1:c.-48-4116G>A	NP_001362399.1:n.-48-4116G>A