Canonical Allele Identifier: CA1505231299
Gene: NPY2R HGNC NCBI

Linked Data

dbSNP Id: rs1729363153

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.155209752C>G , CM000666.2:g.155209752C>G GRCh38
NC_000004.11:g.156130904C>G , CM000666.1:g.156130904C>G GRCh37
NC_000004.10:g.156350354C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000329476.4:c.-49+683C>G MANE Select ENSP00000332591.3:n.-49+683C>G
ENST00000329476.3:c.-49+683C>G ENSP00000332591.3:n.-49+683C>G
ENST00000506608.1:c.-49+687C>G ENSP00000426366.1:n.-49+687C>G
NM_000910.3:c.-49+683C>G NP_000901.1:n.-49+683C>G
XM_005263033.3:c.-48-4140C>G XP_005263090.1:n.-48-4140C>G
XM_005263034.3:c.-49+687C>G XP_005263091.1:n.-49+687C>G
XM_005263033.4:c.-48-4140C>G XP_005263090.1:n.-48-4140C>G
XM_005263034.4:c.-49+687C>G XP_005263091.1:n.-49+687C>G
NM_000910.4:c.-49+683C>G MANE Select NP_000901.1:n.-49+683C>G
NM_001370180.1:c.-49+687C>G NP_001357109.1:n.-49+687C>G
NM_001375470.1:c.-48-4140C>G NP_001362399.1:n.-48-4140C>G