Canonical Allele Identifier: CA1505231306

Gene: NPY2R

Linked Data

• dbSNP Id: rs1578898442

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.155209766A>G , CM000666.2:g.155209766A>G	GRCh38
NC_000004.11:g.156130918A>G , CM000666.1:g.156130918A>G	GRCh37
NC_000004.10:g.156350368A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329476.4:c.-49+697A>G MANE Select	ENSP00000332591.3:n.-49+697A>G
ENST00000329476.3:c.-49+697A>G	ENSP00000332591.3:n.-49+697A>G
ENST00000506608.1:c.-49+701A>G	ENSP00000426366.1:n.-49+701A>G
NM_000910.3:c.-49+697A>G	NP_000901.1:n.-49+697A>G
XM_005263033.3:c.-48-4126A>G	XP_005263090.1:n.-48-4126A>G
XM_005263034.3:c.-49+701A>G	XP_005263091.1:n.-49+701A>G
XM_005263033.4:c.-48-4126A>G	XP_005263090.1:n.-48-4126A>G
XM_005263034.4:c.-49+701A>G	XP_005263091.1:n.-49+701A>G
NM_000910.4:c.-49+697A>G MANE Select	NP_000901.1:n.-49+697A>G
NM_001370180.1:c.-49+701A>G	NP_001357109.1:n.-49+701A>G
NM_001375470.1:c.-48-4126A>G	NP_001362399.1:n.-48-4126A>G