Canonical Allele Identifier: CA2716877534

Gene: PEBP4

Linked Data

• dbSNP Id: rs2128756010

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.22786133A>G , CM000670.2:g.22786133A>G	GRCh38
NC_000008.10:g.22643646A>G , CM000670.1:g.22643646A>G	GRCh37
NC_000008.9:g.22699591A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000256404.8:c.357+31504T>C MANE Select	ENSP00000256404.6:n.357+31504T>C
ENST00000256404.7:c.357+31504T>C	ENSP00000256404.6:n.357+31504T>C
NM_144962.2:c.357+31504T>C	NP_659399.2:n.357+31504T>C
XM_011544413.1:c.357+31504T>C	XP_011542715.1:n.357+31504T>C
XM_011544414.1:c.357+31504T>C	XP_011542716.1:n.357+31504T>C
NM_001363233.1:c.357+31504T>C	NP_001350162.1:n.357+31504T>C
NM_144962.3:c.357+31504T>C MANE Select	NP_659399.2:n.357+31504T>C
NM_001363233.2:c.357+31504T>C	NP_001350162.1:n.357+31504T>C