Canonical Allele Identifier: CA8594921

Gene: PYY

Linked Data

• dbSNP Id: rs770863074
• ExAC: 17:42030294 G / A
• gnomAD v2: 17-42030294-G-A
• gnomAD v4: 17-43952926-G-A
• MyVariant Identifiers: chr17:g.42030294G>A (hg19) ; chr17:g.43952926G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43952926G>A , CM000679.2:g.43952926G>A	GRCh38
NC_000017.10:g.42030294G>A , CM000679.1:g.42030294G>A	GRCh37
NC_000017.9:g.39385820G>A	NCBI36
NG_023338.1:g.56544C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592796.2:c.*179C>T	ENSP00000467310.1:n.*179C>T
ENST00000692052.1:c.*30C>T MANE Select	ENSP00000509262.1:n.*30C>T
ENST00000360085.6:c.*30C>T	ENSP00000353198.1:n.*30C>T
ENST00000592796.1:c.*179C>T	ENSP00000467310.1:n.*179C>T
NM_004160.4:c.*30C>T	NP_004151.3:n.*30C>T
XM_011525035.1:c.*30C>T	XP_011523337.1:n.*30C>T
NM_004160.5:c.*30C>T	NP_004151.3:n.*30C>T
NM_001394028.1:c.*30C>T MANE Select	NP_001380957.1:n.*30C>T
NM_001394029.1:c.*179C>T	NP_001380958.1:n.*179C>T
NM_004160.6:c.*30C>T	NP_004151.4:n.*30C>T