Canonical Allele Identifier: CA2638142793
Gene: PYY HGNC NCBI

Linked Data

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

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

Transcript Alleles

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