Canonical Allele Identifier: CA849939064
Gene: PEBP4 HGNC NCBI

Linked Data

dbSNP Id: rs1381042923
gnomAD v3: 8-22786145-A-C
gnomAD v4: 8-22786145-A-C
MyVariant Identifiers: chr8:g.22643658A>C (hg19) chr8:g.22786145A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.22786145A>C , CM000670.2:g.22786145A>C GRCh38
NC_000008.10:g.22643658A>C , CM000670.1:g.22643658A>C GRCh37
NC_000008.9:g.22699603A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000256404.8:c.357+31492T>G MANE Select ENSP00000256404.6:n.357+31492T>G
ENST00000256404.7:c.357+31492T>G ENSP00000256404.6:n.357+31492T>G
NM_144962.2:c.357+31492T>G NP_659399.2:n.357+31492T>G
XM_011544413.1:c.357+31492T>G XP_011542715.1:n.357+31492T>G
XM_011544414.1:c.357+31492T>G XP_011542716.1:n.357+31492T>G
NM_001363233.1:c.357+31492T>G NP_001350162.1:n.357+31492T>G
NM_144962.3:c.357+31492T>G MANE Select NP_659399.2:n.357+31492T>G
NM_001363233.2:c.357+31492T>G NP_001350162.1:n.357+31492T>G
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