Canonical Allele Identifier: CA790184386
Gene: NPY1R HGNC NCBI

Linked Data

dbSNP Id: rs1468391317
MyVariant Identifiers: chr4:g.164245678A>G (hg19) chr4:g.163324526A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.163324526A>G , CM000666.2:g.163324526A>G GRCh38
NC_000004.11:g.164245678A>G , CM000666.1:g.164245678A>G GRCh37
NC_000004.10:g.164465128A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296533.3:c.*777T>C MANE Select ENSP00000354652.2:n.*777T>C
ENST00000296533.2:c.*777T>C ENSP00000354652.2:n.*777T>C
NM_000909.5:c.*777T>C NP_000900.1:n.*777T>C
XM_005263031.2:c.*777T>C XP_005263088.1:n.*777T>C
XM_011532010.1:c.*777T>C XP_011530312.1:n.*777T>C
XM_005263031.4:c.*777T>C XP_005263088.1:n.*777T>C
XM_011532010.3:c.*777T>C XP_011530312.1:n.*777T>C
NM_000909.6:c.*777T>C MANE Select NP_000900.1:n.*777T>C
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