Canonical Allele Identifier: CA11704949

Gene: NPY2R

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.155204181C>A , CM000666.2:g.155204181C>A	GRCh38
NC_000004.11:g.156125333C>A , CM000666.1:g.156125333C>A	GRCh37
NC_000004.10:g.156344783C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_005263033.3:c.-48-9711C>A	XP_005263090.1:n.-48-9711C>A
XM_005263033.4:c.-48-9711C>A	XP_005263090.1:n.-48-9711C>A
NM_001375470.1:c.-48-9711C>A	NP_001362399.1:n.-48-9711C>A