Canonical Allele Identifier: CA108984808

Gene: NPY2R

Linked Data

• dbSNP Id: rs148092972
• gnomAD v3: 4-155209781-A-T
• gnomAD v4: 4-155209781-A-T
• MyVariant Identifiers: chr4:g.156130933A>T (hg19) ; chr4:g.155209781A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.155209781A>T , CM000666.2:g.155209781A>T	GRCh38
NC_000004.11:g.156130933A>T , CM000666.1:g.156130933A>T	GRCh37
NC_000004.10:g.156350383A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329476.4:c.-49+712A>T MANE Select	ENSP00000332591.3:n.-49+712A>T
ENST00000329476.3:c.-49+712A>T	ENSP00000332591.3:n.-49+712A>T
ENST00000506608.1:c.-49+716A>T	ENSP00000426366.1:n.-49+716A>T
NM_000910.3:c.-49+712A>T	NP_000901.1:n.-49+712A>T
XM_005263033.3:c.-48-4111A>T	XP_005263090.1:n.-48-4111A>T
XM_005263034.3:c.-49+716A>T	XP_005263091.1:n.-49+716A>T
XM_005263033.4:c.-48-4111A>T	XP_005263090.1:n.-48-4111A>T
XM_005263034.4:c.-49+716A>T	XP_005263091.1:n.-49+716A>T
NM_000910.4:c.-49+712A>T MANE Select	NP_000901.1:n.-49+712A>T
NM_001370180.1:c.-49+716A>T	NP_001357109.1:n.-49+716A>T
NM_001375470.1:c.-48-4111A>T	NP_001362399.1:n.-48-4111A>T