Canonical Allele Identifier: CA2638142800
Gene: PYY HGNC NCBI

Linked Data

gnomAD v4: 17-43952816-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43952816G>A , CM000679.2:g.43952816G>A GRCh38
NC_000017.10:g.42030184G>A , CM000679.1:g.42030184G>A GRCh37
NC_000017.9:g.39385710G>A NCBI36
NG_023338.1:g.56654C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000592796.2:c.*289C>T ENSP00000467310.1:n.*289C>T
ENST00000692052.1:c.*140C>T MANE Select ENSP00000509262.1:n.*140C>T
ENST00000360085.6:c.*140C>T ENSP00000353198.1:n.*140C>T
NM_004160.4:c.*140C>T NP_004151.3:n.*140C>T
XM_011525035.1:c.*140C>T XP_011523337.1:n.*140C>T
NM_004160.5:c.*140C>T NP_004151.3:n.*140C>T
NM_001394028.1:c.*140C>T MANE Select NP_001380957.1:n.*140C>T
NM_001394029.1:c.*289C>T NP_001380958.1:n.*289C>T
NM_004160.6:c.*140C>T NP_004151.4:n.*140C>T
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