Canonical Allele Identifier: CA108984811

Gene: NPY2R

Linked Data

• dbSNP Id: rs541644562
• gnomAD v3: 4-155209810-A-C
• gnomAD v4: 4-155209810-A-C
• MyVariant Identifiers: chr4:g.156130962A>C (hg19) ; chr4:g.155209810A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.155209810A>C , CM000666.2:g.155209810A>C	GRCh38
NC_000004.11:g.156130962A>C , CM000666.1:g.156130962A>C	GRCh37
NC_000004.10:g.156350412A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000329476.4:c.-49+741A>C MANE Select	ENSP00000332591.3:n.-49+741A>C
ENST00000329476.3:c.-49+741A>C	ENSP00000332591.3:n.-49+741A>C
ENST00000506608.1:c.-49+745A>C	ENSP00000426366.1:n.-49+745A>C
NM_000910.3:c.-49+741A>C	NP_000901.1:n.-49+741A>C
XM_005263033.3:c.-48-4082A>C	XP_005263090.1:n.-48-4082A>C
XM_005263034.3:c.-49+745A>C	XP_005263091.1:n.-49+745A>C
XM_005263033.4:c.-48-4082A>C	XP_005263090.1:n.-48-4082A>C
XM_005263034.4:c.-49+745A>C	XP_005263091.1:n.-49+745A>C
NM_000910.4:c.-49+741A>C MANE Select	NP_000901.1:n.-49+741A>C
NM_001370180.1:c.-49+745A>C	NP_001357109.1:n.-49+745A>C
NM_001375470.1:c.-48-4082A>C	NP_001362399.1:n.-48-4082A>C