Canonical Allele Identifier: CA555862782
Gene: NPY2R HGNC NCBI

Linked Data

dbSNP Id: rs1313094507
gnomAD v2: 4-156130958-G-C
gnomAD v3: 4-155209806-G-C
gnomAD v4: 4-155209806-G-C
MyVariant Identifiers: chr4:g.156130958G>C (hg19) chr4:g.155209806G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.155209806G>C , CM000666.2:g.155209806G>C GRCh38
NC_000004.11:g.156130958G>C , CM000666.1:g.156130958G>C GRCh37
NC_000004.10:g.156350408G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000329476.4:c.-49+737G>C MANE Select ENSP00000332591.3:n.-49+737G>C
ENST00000329476.3:c.-49+737G>C ENSP00000332591.3:n.-49+737G>C
ENST00000506608.1:c.-49+741G>C ENSP00000426366.1:n.-49+741G>C
NM_000910.3:c.-49+737G>C NP_000901.1:n.-49+737G>C
XM_005263033.3:c.-48-4086G>C XP_005263090.1:n.-48-4086G>C
XM_005263034.3:c.-49+741G>C XP_005263091.1:n.-49+741G>C
XM_005263033.4:c.-48-4086G>C XP_005263090.1:n.-48-4086G>C
XM_005263034.4:c.-49+741G>C XP_005263091.1:n.-49+741G>C
NM_000910.4:c.-49+737G>C MANE Select NP_000901.1:n.-49+737G>C
NM_001370180.1:c.-49+741G>C NP_001357109.1:n.-49+741G>C
NM_001375470.1:c.-48-4086G>C NP_001362399.1:n.-48-4086G>C
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