Canonical Allele Identifier: CA8594953

Gene: PYY

Linked Data

• dbSNP Id: rs753380557
• ExAC: 17:42030491 G / T
• gnomAD v2: 17-42030491-G-T
• gnomAD v4: 17-43953123-G-T
• MyVariant Identifiers: chr17:g.42030491G>T (hg19) ; chr17:g.43953123G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43953123G>T , CM000679.2:g.43953123G>T	GRCh38
NC_000017.10:g.42030491G>T , CM000679.1:g.42030491G>T	GRCh37
NC_000017.9:g.39386017G>T	NCBI36
NG_023338.1:g.56347C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592796.2:c.255C>A	ENSP00000467310.1:p.Arg85=
ENST00000692052.1:c.255C>A MANE Select	ENSP00000509262.1:p.Arg85=
ENST00000360085.6:c.255C>A	ENSP00000353198.1:p.Arg85=
ENST00000592796.1:c.255C>A	ENSP00000467310.1:p.Arg85=
NM_004160.4:c.255C>A	NP_004151.3:p.Arg85=
XM_011525035.1:c.255C>A	XP_011523337.1:p.Arg85=
NM_004160.5:c.255C>A	NP_004151.3:p.Arg85=
NM_001394028.1:c.255C>A MANE Select	NP_001380957.1:p.Arg85=
NM_001394029.1:c.255C>A	NP_001380958.1:p.Arg85=
NM_004160.6:c.255C>A	NP_004151.4:p.Arg85=