Canonical Allele Identifier: CA8594960
Gene: PYY HGNC NCBI

Linked Data

dbSNP Id: rs756237443

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43953133C>A , CM000679.2:g.43953133C>A GRCh38
NC_000017.10:g.42030501C>A , CM000679.1:g.42030501C>A GRCh37
NC_000017.9:g.39386027C>A NCBI36
NG_023338.1:g.56337G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000592796.2:c.245G>T ENSP00000467310.1:p.Gly82Val
ENST00000692052.1:c.245G>T MANE Select ENSP00000509262.1:p.Gly82Val
ENST00000360085.6:c.245G>T ENSP00000353198.1:p.Gly82Val
ENST00000592796.1:c.245G>T ENSP00000467310.1:p.Gly82Val
NM_004160.4:c.245G>T NP_004151.3:p.Gly82Val
XM_011525035.1:c.245G>T XP_011523337.1:p.Gly82Val
NM_004160.5:c.245G>T NP_004151.3:p.Gly82Val
NM_001394028.1:c.245G>T MANE Select NP_001380957.1:p.Gly82Val
NM_001394029.1:c.245G>T NP_001380958.1:p.Gly82Val
NM_004160.6:c.245G>T NP_004151.4:p.Gly82Val