Canonical Allele Identifier: CA1770581721

Gene: PEBP4

Linked Data

• dbSNP Id: rs1806022277

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.22786136G>C , CM000670.2:g.22786136G>C	GRCh38
NC_000008.10:g.22643649G>C , CM000670.1:g.22643649G>C	GRCh37
NC_000008.9:g.22699594G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000256404.8:c.357+31501C>G MANE Select	ENSP00000256404.6:n.357+31501C>G
ENST00000256404.7:c.357+31501C>G	ENSP00000256404.6:n.357+31501C>G
NM_144962.2:c.357+31501C>G	NP_659399.2:n.357+31501C>G
XM_011544413.1:c.357+31501C>G	XP_011542715.1:n.357+31501C>G
XM_011544414.1:c.357+31501C>G	XP_011542716.1:n.357+31501C>G
NM_001363233.1:c.357+31501C>G	NP_001350162.1:n.357+31501C>G
NM_144962.3:c.357+31501C>G MANE Select	NP_659399.2:n.357+31501C>G
NM_001363233.2:c.357+31501C>G	NP_001350162.1:n.357+31501C>G