Canonical Allele Identifier: CA500612465

Gene: PYY

Linked Data

• MyVariant Identifiers: chr17:g.42030491G>C (hg19)

Genomic Alleles

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

Transcript Alleles

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