Canonical Allele Identifier: CA983959745
Gene: PYY HGNC NCBI

Linked Data

dbSNP Id: rs2048639871
gnomAD v3: 17-43952818-G-C
gnomAD v4: 17-43952818-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43952818G>C , CM000679.2:g.43952818G>C GRCh38
NC_000017.10:g.42030186G>C , CM000679.1:g.42030186G>C GRCh37
NC_000017.9:g.39385712G>C NCBI36
NG_023338.1:g.56652C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000592796.2:c.*287C>G ENSP00000467310.1:n.*287C>G
ENST00000692052.1:c.*138C>G MANE Select ENSP00000509262.1:n.*138C>G
ENST00000360085.6:c.*138C>G ENSP00000353198.1:n.*138C>G
NM_004160.4:c.*138C>G NP_004151.3:n.*138C>G
XM_011525035.1:c.*138C>G XP_011523337.1:n.*138C>G
NM_004160.5:c.*138C>G NP_004151.3:n.*138C>G
NM_001394028.1:c.*138C>G MANE Select NP_001380957.1:n.*138C>G
NM_001394029.1:c.*287C>G NP_001380958.1:n.*287C>G
NM_004160.6:c.*138C>G NP_004151.4:n.*138C>G
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