Canonical Allele Identifier: CA399727543
Gene: PYY HGNC NCBI

Linked Data

dbSNP Id: rs1446433216

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43953125G>C , CM000679.2:g.43953125G>C GRCh38
NC_000017.10:g.42030493G>C , CM000679.1:g.42030493G>C GRCh37
NC_000017.9:g.39386019G>C NCBI36
NG_023338.1:g.56345C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000592796.2:c.253C>G ENSP00000467310.1:p.Arg85Gly
ENST00000692052.1:c.253C>G MANE Select ENSP00000509262.1:p.Arg85Gly
ENST00000360085.6:c.253C>G ENSP00000353198.1:p.Arg85Gly
ENST00000592796.1:c.253C>G ENSP00000467310.1:p.Arg85Gly
NM_004160.4:c.253C>G NP_004151.3:p.Arg85Gly
XM_011525035.1:c.253C>G XP_011523337.1:p.Arg85Gly
NM_004160.5:c.253C>G NP_004151.3:p.Arg85Gly
NM_001394028.1:c.253C>G MANE Select NP_001380957.1:p.Arg85Gly
NM_001394029.1:c.253C>G NP_001380958.1:p.Arg85Gly
NM_004160.6:c.253C>G NP_004151.4:p.Arg85Gly