Canonical Allele Identifier: CA2261157307
Community Standard Title: NC_000017.11:g.43953963C=
Gene: PYY HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43953963C= , CM000679.2:g.43953963C= GRCh38
NC_000017.10:g.42031331C= , CM000679.1:g.42031331C= GRCh37
NC_000017.9:g.39386857C= NCBI36
NG_023338.1:g.55507G=

Transcript Alleles

HGVS Amino-acid Change
NM_004160.4:c.-114G= NP_004151.3:n.-114G=
NM_004160.5:c.-114G= NP_004151.3:n.-114G=
NM_004160.6:c.-114G= NP_004151.4:n.-114G=
ENST00000360085.6:c.-114G= ENSP00000353198.1:n.-114G=
XM_011525035.1:c.-114G= XP_011523337.1:n.-114G=