Canonical Allele Identifier: CA2638142664
Gene: PYY HGNC NCBI

Linked Data

gnomAD v4: 17-43952749-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43952749T>G , CM000679.2:g.43952749T>G GRCh38
NC_000017.10:g.42030117T>G , CM000679.1:g.42030117T>G GRCh37
NC_000017.9:g.39385643T>G NCBI36
NG_023338.1:g.56721A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000592796.2:c.*356A>C ENSP00000467310.1:n.*356A>C
ENST00000692052.1:c.*207A>C MANE Select ENSP00000509262.1:n.*207A>C
ENST00000360085.6:c.*207A>C ENSP00000353198.1:n.*207A>C
NM_004160.4:c.*207A>C NP_004151.3:n.*207A>C
XM_011525035.1:c.*207A>C XP_011523337.1:n.*207A>C
NM_004160.5:c.*207A>C NP_004151.3:n.*207A>C
NM_001394028.1:c.*207A>C MANE Select NP_001380957.1:n.*207A>C
NM_001394029.1:c.*356A>C NP_001380958.1:n.*356A>C
NM_004160.6:c.*207A>C NP_004151.4:n.*207A>C
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