Canonical Allele Identifier: CA110082136
Gene: NPY1R HGNC NCBI

Linked Data

dbSNP Id: rs1024767801
gnomAD v3: 4-163324655-G-C
gnomAD v4: 4-163324655-G-C
MyVariant Identifiers: chr4:g.164245807G>C (hg19) chr4:g.163324655G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.163324655G>C , CM000666.2:g.163324655G>C GRCh38
NC_000004.11:g.164245807G>C , CM000666.1:g.164245807G>C GRCh37
NC_000004.10:g.164465257G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000296533.3:c.*648C>G MANE Select ENSP00000354652.2:n.*648C>G
ENST00000296533.2:c.*648C>G ENSP00000354652.2:n.*648C>G
NM_000909.5:c.*648C>G NP_000900.1:n.*648C>G
XM_005263031.2:c.*648C>G XP_005263088.1:n.*648C>G
XM_011532010.1:c.*648C>G XP_011530312.1:n.*648C>G
XM_005263031.4:c.*648C>G XP_005263088.1:n.*648C>G
XM_011532010.3:c.*648C>G XP_011530312.1:n.*648C>G
NM_000909.6:c.*648C>G MANE Select NP_000900.1:n.*648C>G
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