Canonical Allele Identifier: CA11666435

Gene: NPY1R

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.163335583A>G , CM000666.2:g.163335583A>G	GRCh38
NC_000004.11:g.164256735A>G , CM000666.1:g.164256735A>G	GRCh37
NC_000004.10:g.164476185A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000511901.1:c.-152+8722T>C	ENSP00000423878.1:n.-152+8722T>C
XM_005263031.2:c.-152+8722T>C	XP_005263088.1:n.-152+8722T>C
XM_005263031.4:c.-152+8722T>C	XP_005263088.1:n.-152+8722T>C