Canonical Allele Identifier: CA110082129
Gene: NPY1R HGNC NCBI

Linked Data

dbSNP Id: rs1037851710
gnomAD v3: 4-163324603-C-T
gnomAD v4: 4-163324603-C-T
MyVariant Identifiers: chr4:g.164245755C>T (hg19) chr4:g.163324603C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.163324603C>T , CM000666.2:g.163324603C>T GRCh38
NC_000004.11:g.164245755C>T , CM000666.1:g.164245755C>T GRCh37
NC_000004.10:g.164465205C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000296533.3:c.*700G>A MANE Select ENSP00000354652.2:n.*700G>A
ENST00000296533.2:c.*700G>A ENSP00000354652.2:n.*700G>A
NM_000909.5:c.*700G>A NP_000900.1:n.*700G>A
XM_005263031.2:c.*700G>A XP_005263088.1:n.*700G>A
XM_011532010.1:c.*700G>A XP_011530312.1:n.*700G>A
XM_005263031.4:c.*700G>A XP_005263088.1:n.*700G>A
XM_011532010.3:c.*700G>A XP_011530312.1:n.*700G>A
NM_000909.6:c.*700G>A MANE Select NP_000900.1:n.*700G>A
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