Canonical Allele Identifier: CA1024571144
Gene: PIWIL3 HGNC NCBI

Linked Data

dbSNP Id: rs1924532397
gnomAD v3: 22-24748878-A-G
gnomAD v4: 22-24748878-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.24748878A>G , CM000684.2:g.24748878A>G GRCh38
NC_000022.10:g.25144845A>G , CM000684.1:g.25144845A>G GRCh37
NC_000022.9:g.23474845A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000527701.6:c.*1421+29T>C ENSP00000435718.2:n.*1421+29T>C
ENST00000533313.6:c.*1375+29T>C ENSP00000431843.2:n.*1375+29T>C
ENST00000616349.5:c.1449+29T>C MANE Select ENSP00000479524.2:n.1449+29T>C
ENST00000332271.9:c.1449+29T>C ENSP00000330031.5:n.1449+29T>C
ENST00000527701.5:c.1122+29T>C ENSP00000435718.1:n.1122+29T>C
ENST00000532537.2:n.1870+29T>C
ENST00000533313.5:c.1122+29T>C ENSP00000431843.1:n.1122+29T>C
ENST00000616349.4:c.1449+29T>C ENSP00000479524.1:n.1449+29T>C
NM_001008496.3:c.1449+29T>C NP_001008496.2:n.1449+29T>C
NM_001255975.1:c.1449+29T>C MANE Select NP_001242904.1:n.1449+29T>C
NR_045648.1:n.2080+29T>C
NR_045649.1:n.1953+29T>C
NR_045649.2:n.1953+29T>C
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