Canonical Allele Identifier: CA8594946

Gene: PYY

Linked Data

• dbSNP Id: rs768287479
• ExAC: 17:42030447 T / G
• gnomAD v2: 17-42030447-T-G
• gnomAD v4: 17-43953079-T-G
• MyVariant Identifiers: chr17:g.42030447T>G (hg19) ; chr17:g.43953079T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43953079T>G , CM000679.2:g.43953079T>G	GRCh38
NC_000017.10:g.42030447T>G , CM000679.1:g.42030447T>G	GRCh37
NC_000017.9:g.39385973T>G	NCBI36
NG_023338.1:g.56391A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592796.2:c.*26A>C	ENSP00000467310.1:n.*26A>C
ENST00000692052.1:c.269+30A>C MANE Select	ENSP00000509262.1:n.269+30A>C
ENST00000360085.6:c.269+30A>C	ENSP00000353198.1:n.269+30A>C
ENST00000592796.1:c.*26A>C	ENSP00000467310.1:n.*26A>C
NM_004160.4:c.269+30A>C	NP_004151.3:n.269+30A>C
XM_011525035.1:c.269+30A>C	XP_011523337.1:n.269+30A>C
NM_004160.5:c.269+30A>C	NP_004151.3:n.269+30A>C
NM_001394028.1:c.269+30A>C MANE Select	NP_001380957.1:n.269+30A>C
NM_001394029.1:c.*26A>C	NP_001380958.1:n.*26A>C
NM_004160.6:c.269+30A>C	NP_004151.4:n.269+30A>C