Canonical Allele Identifier: CA8594928
Gene: PYY HGNC NCBI

Linked Data

dbSNP Id: rs201282783

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43952960C>T , CM000679.2:g.43952960C>T GRCh38
NC_000017.10:g.42030328C>T , CM000679.1:g.42030328C>T GRCh37
NC_000017.9:g.39385854C>T NCBI36
NG_023338.1:g.56510G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000592796.2:c.*145G>A ENSP00000467310.1:n.*145G>A
ENST00000692052.1:c.290G>A MANE Select ENSP00000509262.1:p.Trp97Ter
ENST00000360085.6:c.290G>A ENSP00000353198.1:p.Trp97Ter
ENST00000592796.1:c.*145G>A ENSP00000467310.1:n.*145G>A
NM_004160.4:c.290G>A NP_004151.3:p.Trp97Ter
XM_011525035.1:c.290G>A XP_011523337.1:p.Trp97Ter
NM_004160.5:c.290G>A NP_004151.3:p.Trp97Ter
NM_001394028.1:c.290G>A MANE Select NP_001380957.1:p.Trp97Ter
NM_001394029.1:c.*145G>A NP_001380958.1:n.*145G>A
NM_004160.6:c.290G>A NP_004151.4:p.Trp97Ter