Canonical Allele Identifier: CA8594929

Gene: PYY

Linked Data

• dbSNP Id: rs761833484
• ExAC: 17:42030329 A / G
• gnomAD v2: 17-42030329-A-G
• MyVariant Identifiers: chr17:g.42030329A>G (hg19) ; chr17:g.43952961A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43952961A>G , CM000679.2:g.43952961A>G	GRCh38
NC_000017.10:g.42030329A>G , CM000679.1:g.42030329A>G	GRCh37
NC_000017.9:g.39385855A>G	NCBI36
NG_023338.1:g.56509T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592796.2:c.*144T>C	ENSP00000467310.1:n.*144T>C
ENST00000692052.1:c.289T>C MANE Select	ENSP00000509262.1:p.Trp97Arg
ENST00000360085.6:c.289T>C	ENSP00000353198.1:p.Trp97Arg
ENST00000592796.1:c.*144T>C	ENSP00000467310.1:n.*144T>C
NM_004160.4:c.289T>C	NP_004151.3:p.Trp97Arg
XM_011525035.1:c.289T>C	XP_011523337.1:p.Trp97Arg
NM_004160.5:c.289T>C	NP_004151.3:p.Trp97Arg
NM_001394028.1:c.289T>C MANE Select	NP_001380957.1:p.Trp97Arg
NM_001394029.1:c.*144T>C	NP_001380958.1:n.*144T>C
NM_004160.6:c.289T>C	NP_004151.4:p.Trp97Arg