Canonical Allele Identifier: CA2638142794
Gene: PYY HGNC NCBI

Linked Data

gnomAD v4: 17-43952813-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43952813A>C , CM000679.2:g.43952813A>C GRCh38
NC_000017.10:g.42030181A>C , CM000679.1:g.42030181A>C GRCh37
NC_000017.9:g.39385707A>C NCBI36
NG_023338.1:g.56657T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000592796.2:c.*292T>G ENSP00000467310.1:n.*292T>G
ENST00000692052.1:c.*143T>G MANE Select ENSP00000509262.1:n.*143T>G
ENST00000360085.6:c.*143T>G ENSP00000353198.1:n.*143T>G
NM_004160.4:c.*143T>G NP_004151.3:n.*143T>G
XM_011525035.1:c.*143T>G XP_011523337.1:n.*143T>G
NM_004160.5:c.*143T>G NP_004151.3:n.*143T>G
NM_001394028.1:c.*143T>G MANE Select NP_001380957.1:n.*143T>G
NM_001394029.1:c.*292T>G NP_001380958.1:n.*292T>G
NM_004160.6:c.*143T>G NP_004151.4:n.*143T>G
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