Canonical Allele Identifier: CA2716877537
Gene: PEBP4 HGNC NCBI

Linked Data

dbSNP Id: rs2128756017
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.22786152T>C , CM000670.2:g.22786152T>C GRCh38
NC_000008.10:g.22643665T>C , CM000670.1:g.22643665T>C GRCh37
NC_000008.9:g.22699610T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256404.8:c.357+31485A>G MANE Select ENSP00000256404.6:n.357+31485A>G
ENST00000256404.7:c.357+31485A>G ENSP00000256404.6:n.357+31485A>G
NM_144962.2:c.357+31485A>G NP_659399.2:n.357+31485A>G
XM_011544413.1:c.357+31485A>G XP_011542715.1:n.357+31485A>G
XM_011544414.1:c.357+31485A>G XP_011542716.1:n.357+31485A>G
NM_001363233.1:c.357+31485A>G NP_001350162.1:n.357+31485A>G
NM_144962.3:c.357+31485A>G MANE Select NP_659399.2:n.357+31485A>G
NM_001363233.2:c.357+31485A>G NP_001350162.1:n.357+31485A>G
Search 100 bp 5'
Search 100 bp 3'