Canonical Allele Identifier: CA155829828

Gene: NPY

Linked Data

• dbSNP Id: rs566223932
• gnomAD v2: 7-24331484-G-A
• gnomAD v3: 7-24291865-G-A
• gnomAD v4: 7-24291865-G-A
• MyVariant Identifiers: chr7:g.24331484G>A (hg19) ; chr7:g.24291865G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24291865G>A , CM000669.2:g.24291865G>A	GRCh38
NC_000007.13:g.24331484G>A , CM000669.1:g.24331484G>A	GRCh37
NC_000007.12:g.24298009G>A	NCBI36
NG_016148.1:g.12678G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.6:c.*178G>A	ENSP00000242152.2:n.*178G>A
NM_000905.3:c.*178G>A	NP_000896.1:n.*178G>A
XM_017012910.1:c.41+27492C>T	XP_016868399.1:n.41+27492C>T
XM_017012911.1:c.41+27492C>T	XP_016868400.1:n.41+27492C>T
XR_001745121.1:n.473+27492C>T
XR_001745122.1:n.345-94836C>T
XR_001745123.1:n.473+27492C>T
XR_001745124.1:n.473+27492C>T
XR_001745125.1:n.473+27492C>T
XR_001745126.1:n.473+27492C>T
XR_001745127.1:n.345-36166C>T
XR_001745129.1:n.473+27492C>T
XR_001745130.1:n.473+27492C>T
XR_001745131.1:n.473+27492C>T
XR_001745132.1:n.473+27492C>T