Canonical Allele Identifier: CA772250283

Gene: PYY

Linked Data

• dbSNP Id: rs1406198610
• gnomAD v3: 17-43953075-C-T
• gnomAD v4: 17-43953075-C-T
• MyVariant Identifiers: chr17:g.42030443C>T (hg19) ; chr17:g.43953075C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43953075C>T , CM000679.2:g.43953075C>T	GRCh38
NC_000017.10:g.42030443C>T , CM000679.1:g.42030443C>T	GRCh37
NC_000017.9:g.39385969C>T	NCBI36
NG_023338.1:g.56395G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592796.2:c.*30G>A	ENSP00000467310.1:n.*30G>A
ENST00000692052.1:c.269+34G>A MANE Select	ENSP00000509262.1:n.269+34G>A
ENST00000360085.6:c.269+34G>A	ENSP00000353198.1:n.269+34G>A
ENST00000592796.1:c.*30G>A	ENSP00000467310.1:n.*30G>A
NM_004160.4:c.269+34G>A	NP_004151.3:n.269+34G>A
XM_011525035.1:c.269+34G>A	XP_011523337.1:n.269+34G>A
NM_004160.5:c.269+34G>A	NP_004151.3:n.269+34G>A
NM_001394028.1:c.269+34G>A MANE Select	NP_001380957.1:n.269+34G>A
NM_001394029.1:c.*30G>A	NP_001380958.1:n.*30G>A
NM_004160.6:c.269+34G>A	NP_004151.4:n.269+34G>A