Canonical Allele Identifier: CA16206719
Gene: NPY2R HGNC NCBI

Linked Data

dbSNP Id: rs10461257
gnomAD v2: 4-156131004-G-A
gnomAD v3: 4-155209852-G-A
gnomAD v4: 4-155209852-G-A
MyVariant Identifiers: chr4:g.156131004G>A (hg19) chr4:g.155209852G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.155209852G>A , CM000666.2:g.155209852G>A GRCh38
NC_000004.11:g.156131004G>A , CM000666.1:g.156131004G>A GRCh37
NC_000004.10:g.156350454G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000329476.4:c.-49+783G>A MANE Select ENSP00000332591.3:n.-49+783G>A
ENST00000329476.3:c.-49+783G>A ENSP00000332591.3:n.-49+783G>A
ENST00000506608.1:c.-49+787G>A ENSP00000426366.1:n.-49+787G>A
NM_000910.3:c.-49+783G>A NP_000901.1:n.-49+783G>A
XM_005263033.3:c.-48-4040G>A XP_005263090.1:n.-48-4040G>A
XM_005263034.3:c.-49+787G>A XP_005263091.1:n.-49+787G>A
XM_005263033.4:c.-48-4040G>A XP_005263090.1:n.-48-4040G>A
XM_005263034.4:c.-49+787G>A XP_005263091.1:n.-49+787G>A
NM_000910.4:c.-49+783G>A MANE Select NP_000901.1:n.-49+783G>A
NM_001370180.1:c.-49+787G>A NP_001357109.1:n.-49+787G>A
NM_001375470.1:c.-48-4040G>A NP_001362399.1:n.-48-4040G>A
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