Canonical Allele Identifier: CA108984809
Gene: NPY2R HGNC NCBI

Linked Data

dbSNP Id: rs17376826

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.155209796C>T , CM000666.2:g.155209796C>T GRCh38
NC_000004.11:g.156130948C>T , CM000666.1:g.156130948C>T GRCh37
NC_000004.10:g.156350398C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000329476.4:c.-49+727C>T MANE Select ENSP00000332591.3:n.-49+727C>T
ENST00000329476.3:c.-49+727C>T ENSP00000332591.3:n.-49+727C>T
ENST00000506608.1:c.-49+731C>T ENSP00000426366.1:n.-49+731C>T
NM_000910.3:c.-49+727C>T NP_000901.1:n.-49+727C>T
XM_005263033.3:c.-48-4096C>T XP_005263090.1:n.-48-4096C>T
XM_005263034.3:c.-49+731C>T XP_005263091.1:n.-49+731C>T
XM_005263033.4:c.-48-4096C>T XP_005263090.1:n.-48-4096C>T
XM_005263034.4:c.-49+731C>T XP_005263091.1:n.-49+731C>T
NM_000910.4:c.-49+727C>T MANE Select NP_000901.1:n.-49+727C>T
NM_001370180.1:c.-49+731C>T NP_001357109.1:n.-49+731C>T
NM_001375470.1:c.-48-4096C>T NP_001362399.1:n.-48-4096C>T