Canonical Allele Identifier: CA1770581569
Gene: PEBP4 HGNC NCBI

Linked Data

dbSNP Id: rs1806020036
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.22786016G>T , CM000670.2:g.22786016G>T GRCh38
NC_000008.10:g.22643529G>T , CM000670.1:g.22643529G>T GRCh37
NC_000008.9:g.22699474G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256404.8:c.357+31621C>A MANE Select ENSP00000256404.6:n.357+31621C>A
ENST00000256404.7:c.357+31621C>A ENSP00000256404.6:n.357+31621C>A
NM_144962.2:c.357+31621C>A NP_659399.2:n.357+31621C>A
XM_011544413.1:c.357+31621C>A XP_011542715.1:n.357+31621C>A
XM_011544414.1:c.357+31621C>A XP_011542716.1:n.357+31621C>A
NM_001363233.1:c.357+31621C>A NP_001350162.1:n.357+31621C>A
NM_144962.3:c.357+31621C>A MANE Select NP_659399.2:n.357+31621C>A
NM_001363233.2:c.357+31621C>A NP_001350162.1:n.357+31621C>A
Search 100 bp 5'
Search 100 bp 3'