Canonical Allele Identifier: CA399727448
Gene: PYY HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.42030474T>G (hg19) chr17:g.43953106T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43953106T>G , CM000679.2:g.43953106T>G GRCh38
NC_000017.10:g.42030474T>G , CM000679.1:g.42030474T>G GRCh37
NC_000017.9:g.39386000T>G NCBI36
NG_023338.1:g.56364A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000592796.2:c.272A>C ENSP00000467310.1:p.Ter91Ser
ENST00000692052.1:c.269+3A>C MANE Select ENSP00000509262.1:n.269+3A>C
ENST00000360085.6:c.269+3A>C ENSP00000353198.1:n.269+3A>C
ENST00000592796.1:c.272A>C ENSP00000467310.1:p.Ter91Ser
NM_004160.4:c.269+3A>C NP_004151.3:n.269+3A>C
XM_011525035.1:c.269+3A>C XP_011523337.1:n.269+3A>C
NM_004160.5:c.269+3A>C NP_004151.3:n.269+3A>C
NM_001394028.1:c.269+3A>C MANE Select NP_001380957.1:n.269+3A>C
NM_001394029.1:c.272A>C NP_001380958.1:p.Ter91Ser
NM_004160.6:c.269+3A>C NP_004151.4:n.269+3A>C
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