Canonical Allele Identifier: CA500242999
Gene: PYY HGNC NCBI

Linked Data

gnomAD v4: 17-43952962-C-G
MyVariant Identifiers: chr17:g.42030330C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43952962C>G , CM000679.2:g.43952962C>G GRCh38
NC_000017.10:g.42030330C>G , CM000679.1:g.42030330C>G GRCh37
NC_000017.9:g.39385856C>G NCBI36
NG_023338.1:g.56508G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000592796.2:c.*143G>C ENSP00000467310.1:n.*143G>C
ENST00000692052.1:c.288G>C MANE Select ENSP00000509262.1:p.Leu96=
ENST00000360085.6:c.288G>C ENSP00000353198.1:p.Leu96=
ENST00000592796.1:c.*143G>C ENSP00000467310.1:n.*143G>C
NM_004160.4:c.288G>C NP_004151.3:p.Leu96=
XM_011525035.1:c.288G>C XP_011523337.1:p.Leu96=
NM_004160.5:c.288G>C NP_004151.3:p.Leu96=
NM_001394028.1:c.288G>C MANE Select NP_001380957.1:p.Leu96=
NM_001394029.1:c.*143G>C NP_001380958.1:n.*143G>C
NM_004160.6:c.288G>C NP_004151.4:p.Leu96=
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