Canonical Allele Identifier: CA2261156815
Gene: PYY HGNC NCBI

Linked Data

dbSNP Id: rs2048642623
gnomAD v4: 17-43953071-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43953071C>T , CM000679.2:g.43953071C>T GRCh38
NC_000017.10:g.42030439C>T , CM000679.1:g.42030439C>T GRCh37
NC_000017.9:g.39385965C>T NCBI36
NG_023338.1:g.56399G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000592796.2:c.*34G>A ENSP00000467310.1:n.*34G>A
ENST00000692052.1:c.269+38G>A MANE Select ENSP00000509262.1:n.269+38G>A
ENST00000360085.6:c.269+38G>A ENSP00000353198.1:n.269+38G>A
ENST00000592796.1:c.*34G>A ENSP00000467310.1:n.*34G>A
NM_004160.4:c.269+38G>A NP_004151.3:n.269+38G>A
XM_011525035.1:c.269+38G>A XP_011523337.1:n.269+38G>A
NM_004160.5:c.269+38G>A NP_004151.3:n.269+38G>A
NM_001394028.1:c.269+38G>A MANE Select NP_001380957.1:n.269+38G>A
NM_001394029.1:c.*34G>A NP_001380958.1:n.*34G>A
NM_004160.6:c.269+38G>A NP_004151.4:n.269+38G>A
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