Canonical Allele Identifier: CA8594952
Gene: PYY HGNC NCBI

Linked Data

dbSNP Id: rs766105817

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43953121G>T , CM000679.2:g.43953121G>T GRCh38
NC_000017.10:g.42030489G>T , CM000679.1:g.42030489G>T GRCh37
NC_000017.9:g.39386015G>T NCBI36
NG_023338.1:g.56349C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000592796.2:c.257C>A ENSP00000467310.1:p.Pro86His
ENST00000692052.1:c.257C>A MANE Select ENSP00000509262.1:p.Pro86His
ENST00000360085.6:c.257C>A ENSP00000353198.1:p.Pro86His
ENST00000592796.1:c.257C>A ENSP00000467310.1:p.Pro86His
NM_004160.4:c.257C>A NP_004151.3:p.Pro86His
XM_011525035.1:c.257C>A XP_011523337.1:p.Pro86His
NM_004160.5:c.257C>A NP_004151.3:p.Pro86His
NM_001394028.1:c.257C>A MANE Select NP_001380957.1:p.Pro86His
NM_001394029.1:c.257C>A NP_001380958.1:p.Pro86His
NM_004160.6:c.257C>A NP_004151.4:p.Pro86His