Canonical Allele Identifier: CA790184394
Gene: NPY1R HGNC NCBI

Linked Data

dbSNP Id: rs1306804214
gnomAD v3: 4-163324546-T-C
gnomAD v4: 4-163324546-T-C
MyVariant Identifiers: chr4:g.164245698T>C (hg19) chr4:g.163324546T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.163324546T>C , CM000666.2:g.163324546T>C GRCh38
NC_000004.11:g.164245698T>C , CM000666.1:g.164245698T>C GRCh37
NC_000004.10:g.164465148T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296533.3:c.*757A>G MANE Select ENSP00000354652.2:n.*757A>G
ENST00000296533.2:c.*757A>G ENSP00000354652.2:n.*757A>G
NM_000909.5:c.*757A>G NP_000900.1:n.*757A>G
XM_005263031.2:c.*757A>G XP_005263088.1:n.*757A>G
XM_011532010.1:c.*757A>G XP_011530312.1:n.*757A>G
XM_005263031.4:c.*757A>G XP_005263088.1:n.*757A>G
XM_011532010.3:c.*757A>G XP_011530312.1:n.*757A>G
NM_000909.6:c.*757A>G MANE Select NP_000900.1:n.*757A>G
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