Canonical Allele Identifier: CA983959729
Gene: PYY HGNC NCBI

Linked Data

dbSNP Id: rs757523473
gnomAD v4: 17-43952810-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43952810G>T , CM000679.2:g.43952810G>T GRCh38
NC_000017.10:g.42030178G>T , CM000679.1:g.42030178G>T GRCh37
NC_000017.9:g.39385704G>T NCBI36
NG_023338.1:g.56660C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000592796.2:c.*295C>A ENSP00000467310.1:n.*295C>A
ENST00000692052.1:c.*146C>A MANE Select ENSP00000509262.1:n.*146C>A
ENST00000360085.6:c.*146C>A ENSP00000353198.1:n.*146C>A
NM_004160.4:c.*146C>A NP_004151.3:n.*146C>A
XM_011525035.1:c.*146C>A XP_011523337.1:n.*146C>A
NM_004160.5:c.*146C>A NP_004151.3:n.*146C>A
NM_001394028.1:c.*146C>A MANE Select NP_001380957.1:n.*146C>A
NM_001394029.1:c.*295C>A NP_001380958.1:n.*295C>A
NM_004160.6:c.*146C>A NP_004151.4:n.*146C>A
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