Canonical Allele Identifier: CA399727315
Gene: PYY HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.42030334T>C (hg19) chr17:g.43952966T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43952966T>C , CM000679.2:g.43952966T>C GRCh38
NC_000017.10:g.42030334T>C , CM000679.1:g.42030334T>C GRCh37
NC_000017.9:g.39385860T>C NCBI36
NG_023338.1:g.56504A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000592796.2:c.*139A>G ENSP00000467310.1:n.*139A>G
ENST00000692052.1:c.284A>G MANE Select ENSP00000509262.1:p.Asp95Gly
ENST00000360085.6:c.284A>G ENSP00000353198.1:p.Asp95Gly
ENST00000592796.1:c.*139A>G ENSP00000467310.1:n.*139A>G
NM_004160.4:c.284A>G NP_004151.3:p.Asp95Gly
XM_011525035.1:c.284A>G XP_011523337.1:p.Asp95Gly
NM_004160.5:c.284A>G NP_004151.3:p.Asp95Gly
NM_001394028.1:c.284A>G MANE Select NP_001380957.1:p.Asp95Gly
NM_001394029.1:c.*139A>G NP_001380958.1:n.*139A>G
NM_004160.6:c.284A>G NP_004151.4:p.Asp95Gly
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