Canonical Allele Identifier: CA1099401419
Gene: NPY HGNC NCBI

Linked Data

dbSNP Id: rs1787631158
gnomAD v3: 7-24291863-G-A
gnomAD v4: 7-24291863-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24291863G>A , CM000669.2:g.24291863G>A GRCh38
NC_000007.13:g.24331482G>A , CM000669.1:g.24331482G>A GRCh37
NC_000007.12:g.24298007G>A NCBI36
NG_016148.1:g.12676G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000242152.6:c.*176G>A ENSP00000242152.2:n.*176G>A
NM_000905.3:c.*176G>A NP_000896.1:n.*176G>A
XM_017012910.1:c.41+27494C>T XP_016868399.1:n.41+27494C>T
XM_017012911.1:c.41+27494C>T XP_016868400.1:n.41+27494C>T
XR_001745121.1:n.473+27494C>T
XR_001745122.1:n.345-94834C>T
XR_001745123.1:n.473+27494C>T
XR_001745124.1:n.473+27494C>T
XR_001745125.1:n.473+27494C>T
XR_001745126.1:n.473+27494C>T
XR_001745127.1:n.345-36164C>T
XR_001745129.1:n.473+27494C>T
XR_001745130.1:n.473+27494C>T
XR_001745131.1:n.473+27494C>T
XR_001745132.1:n.473+27494C>T