Canonical Allele Identifier: CA772250189

Gene: PYY

Linked Data

• dbSNP Id: rs1317099688
• gnomAD v3: 17-43952880-G-C
• gnomAD v4: 17-43952880-G-C
• MyVariant Identifiers: chr17:g.42030248G>C (hg19) ; chr17:g.43952880G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43952880G>C , CM000679.2:g.43952880G>C	GRCh38
NC_000017.10:g.42030248G>C , CM000679.1:g.42030248G>C	GRCh37
NC_000017.9:g.39385774G>C	NCBI36
NG_023338.1:g.56590C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592796.2:c.*225C>G	ENSP00000467310.1:n.*225C>G
ENST00000692052.1:c.*76C>G MANE Select	ENSP00000509262.1:n.*76C>G
ENST00000360085.6:c.*76C>G	ENSP00000353198.1:n.*76C>G
NM_004160.4:c.*76C>G	NP_004151.3:n.*76C>G
XM_011525035.1:c.*76C>G	XP_011523337.1:n.*76C>G
NM_004160.5:c.*76C>G	NP_004151.3:n.*76C>G
NM_001394028.1:c.*76C>G MANE Select	NP_001380957.1:n.*76C>G
NM_001394029.1:c.*225C>G	NP_001380958.1:n.*225C>G
NM_004160.6:c.*76C>G	NP_004151.4:n.*76C>G