Canonical Allele Identifier: CA442021813

Gene: NPY2R

Linked Data

• dbSNP Id: rs2880415
• MyVariant Identifiers: chr4:g.156136027C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.155214875C>A , CM000666.2:g.155214875C>A	GRCh38
NC_000004.11:g.156136027C>A , CM000666.1:g.156136027C>A	GRCh37
NC_000004.10:g.156355477C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000329476.4:c.936C>A MANE Select	ENSP00000332591.3:p.Ile312=
ENST00000329476.3:c.936C>A	ENSP00000332591.3:p.Ile312=
ENST00000506608.1:c.936C>A	ENSP00000426366.1:p.Ile312=
NM_000910.3:c.936C>A	NP_000901.1:p.Ile312=
XM_005263033.3:c.936C>A	XP_005263090.1:p.Ile312=
XM_005263034.3:c.936C>A	XP_005263091.1:p.Ile312=
XM_005263033.4:c.936C>A	XP_005263090.1:p.Ile312=
XM_005263034.4:c.936C>A	XP_005263091.1:p.Ile312=
NM_000910.4:c.936C>A MANE Select	NP_000901.1:p.Ile312=
NM_001370180.1:c.936C>A	NP_001357109.1:p.Ile312=
NM_001375470.1:c.936C>A	NP_001362399.1:p.Ile312=