Canonical Allele Identifier: CA8594949

Gene: PYY

Linked Data

• dbSNP Id: rs778439432
• ExAC: 17:42030469 G / A
• gnomAD v2: 17-42030469-G-A
• gnomAD v4: 17-43953101-G-A
• MyVariant Identifiers: chr17:g.42030469G>A (hg19) ; chr17:g.43953101G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43953101G>A , CM000679.2:g.43953101G>A	GRCh38
NC_000017.10:g.42030469G>A , CM000679.1:g.42030469G>A	GRCh37
NC_000017.9:g.39385995G>A	NCBI36
NG_023338.1:g.56369C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592796.2:c.*4C>T	ENSP00000467310.1:n.*4C>T
ENST00000692052.1:c.269+8C>T MANE Select	ENSP00000509262.1:n.269+8C>T
ENST00000360085.6:c.269+8C>T	ENSP00000353198.1:n.269+8C>T
ENST00000592796.1:c.*4C>T	ENSP00000467310.1:n.*4C>T
NM_004160.4:c.269+8C>T	NP_004151.3:n.269+8C>T
XM_011525035.1:c.269+8C>T	XP_011523337.1:n.269+8C>T
NM_004160.5:c.269+8C>T	NP_004151.3:n.269+8C>T
NM_001394028.1:c.269+8C>T MANE Select	NP_001380957.1:n.269+8C>T
NM_001394029.1:c.*4C>T	NP_001380958.1:n.*4C>T
NM_004160.6:c.269+8C>T	NP_004151.4:n.269+8C>T