Canonical Allele Identifier: CA2261156651
Gene: PYY HGNC NCBI

Linked Data

dbSNP Id: rs2048639518
gnomAD v4: 17-43952801-G-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43952801G>C , CM000679.2:g.43952801G>C GRCh38
NC_000017.10:g.42030169G>C , CM000679.1:g.42030169G>C GRCh37
NC_000017.9:g.39385695G>C NCBI36
NG_023338.1:g.56669C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000592796.2:c.*304C>G ENSP00000467310.1:n.*304C>G
ENST00000692052.1:c.*155C>G MANE Select ENSP00000509262.1:n.*155C>G
ENST00000360085.6:c.*155C>G ENSP00000353198.1:n.*155C>G
NM_004160.4:c.*155C>G NP_004151.3:n.*155C>G
XM_011525035.1:c.*155C>G XP_011523337.1:n.*155C>G
NM_004160.5:c.*155C>G NP_004151.3:n.*155C>G
NM_001394028.1:c.*155C>G MANE Select NP_001380957.1:n.*155C>G
NM_001394029.1:c.*304C>G NP_001380958.1:n.*304C>G
NM_004160.6:c.*155C>G NP_004151.4:n.*155C>G
Search 100 bp 5'
Search 100 bp 3'