Canonical Allele Identifier: CA2707650247
Gene: NPY1R HGNC NCBI

Linked Data

dbSNP Id: rs2110777386

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.163324800T>C , CM000666.2:g.163324800T>C GRCh38
NC_000004.11:g.164245952T>C , CM000666.1:g.164245952T>C GRCh37
NC_000004.10:g.164465402T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296533.3:c.*503A>G MANE Select ENSP00000354652.2:n.*503A>G
ENST00000296533.2:c.*503A>G ENSP00000354652.2:n.*503A>G
NM_000909.5:c.*503A>G NP_000900.1:n.*503A>G
XM_005263031.2:c.*503A>G XP_005263088.1:n.*503A>G
XM_011532010.1:c.*503A>G XP_011530312.1:n.*503A>G
XM_005263031.4:c.*503A>G XP_005263088.1:n.*503A>G
XM_011532010.3:c.*503A>G XP_011530312.1:n.*503A>G
NM_000909.6:c.*503A>G MANE Select NP_000900.1:n.*503A>G