Canonical Allele Identifier: CA790184433
Gene: NPY1R HGNC NCBI

Linked Data

dbSNP Id: rs1435136492
MyVariant Identifiers: chr4:g.164245820T>C (hg19) chr4:g.163324668T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.163324668T>C , CM000666.2:g.163324668T>C GRCh38
NC_000004.11:g.164245820T>C , CM000666.1:g.164245820T>C GRCh37
NC_000004.10:g.164465270T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000296533.3:c.*635A>G MANE Select ENSP00000354652.2:n.*635A>G
ENST00000296533.2:c.*635A>G ENSP00000354652.2:n.*635A>G
NM_000909.5:c.*635A>G NP_000900.1:n.*635A>G
XM_005263031.2:c.*635A>G XP_005263088.1:n.*635A>G
XM_011532010.1:c.*635A>G XP_011530312.1:n.*635A>G
XM_005263031.4:c.*635A>G XP_005263088.1:n.*635A>G
XM_011532010.3:c.*635A>G XP_011530312.1:n.*635A>G
NM_000909.6:c.*635A>G MANE Select NP_000900.1:n.*635A>G
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