Canonical Allele Identifier: CA173904567
Gene: PEBP4 HGNC NCBI

Linked Data

dbSNP Id: rs999913737
MyVariant Identifiers: chr8:g.22643717A>T (hg19) chr8:g.22786204A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.22786204A>T , CM000670.2:g.22786204A>T GRCh38
NC_000008.10:g.22643717A>T , CM000670.1:g.22643717A>T GRCh37
NC_000008.9:g.22699662A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256404.8:c.357+31433T>A MANE Select ENSP00000256404.6:n.357+31433T>A
ENST00000256404.7:c.357+31433T>A ENSP00000256404.6:n.357+31433T>A
NM_144962.2:c.357+31433T>A NP_659399.2:n.357+31433T>A
XM_011544413.1:c.357+31433T>A XP_011542715.1:n.357+31433T>A
XM_011544414.1:c.357+31433T>A XP_011542716.1:n.357+31433T>A
NM_001363233.1:c.357+31433T>A NP_001350162.1:n.357+31433T>A
NM_144962.3:c.357+31433T>A MANE Select NP_659399.2:n.357+31433T>A
NM_001363233.2:c.357+31433T>A NP_001350162.1:n.357+31433T>A
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