Canonical Allele Identifier: CA820658661
Gene: PPIL4 HGNC NCBI

Linked Data

dbSNP Id: rs9373594
gnomAD v3: 6-149513438-T-A
gnomAD v4: 6-149513438-T-A
MyVariant Identifiers: chr6:g.149834574T>A (hg19) chr6:g.149513438T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.149513438T>A , CM000668.2:g.149513438T>A GRCh38
NC_000006.11:g.149834574T>A , CM000668.1:g.149834574T>A GRCh37
NC_000006.10:g.149876267T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000253329.3:c.1080-1136A>T MANE Select ENSP00000253329.2:n.1080-1136A>T
ENST00000253329.2:c.1080-1136A>T ENSP00000253329.2:n.1080-1136A>T
ENST00000340881.2:c.-23-1136A>T ENSP00000344128.2:n.-23-1136A>T
NM_139126.3:c.1080-1136A>T NP_624311.1:n.1080-1136A>T
NM_139126.4:c.1080-1136A>T MANE Select NP_624311.1:n.1080-1136A>T
Search 100 bp 5'
Search 100 bp 3'