Canonical Allele Identifier: CA110082115
Gene: NPY1R HGNC NCBI

Linked Data

dbSNP Id: rs765491268
gnomAD v3: 4-163324523-A-C
gnomAD v4: 4-163324523-A-C
MyVariant Identifiers: chr4:g.164245675A>C (hg19) chr4:g.163324523A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.163324523A>C , CM000666.2:g.163324523A>C GRCh38
NC_000004.11:g.164245675A>C , CM000666.1:g.164245675A>C GRCh37
NC_000004.10:g.164465125A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296533.3:c.*780T>G MANE Select ENSP00000354652.2:n.*780T>G
ENST00000296533.2:c.*780T>G ENSP00000354652.2:n.*780T>G
NM_000909.5:c.*780T>G NP_000900.1:n.*780T>G
XM_005263031.2:c.*780T>G XP_005263088.1:n.*780T>G
XM_011532010.1:c.*780T>G XP_011530312.1:n.*780T>G
XM_005263031.4:c.*780T>G XP_005263088.1:n.*780T>G
XM_011532010.3:c.*780T>G XP_011530312.1:n.*780T>G
NM_000909.6:c.*780T>G MANE Select NP_000900.1:n.*780T>G
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