Canonical Allele Identifier: CA10529275
Gene: ZIC3 HGNC NCBI

Linked Data

dbSNP Id: rs769295569
ExAC: X:136649006 C / A
gnomAD v2: X-136649006-C-A
gnomAD v3: X-137566847-C-A
gnomAD v4: X-137566847-C-A
MyVariant Identifiers: chrX:g.136649006C>A (hg19) chrX:g.136649006_136649012delinsAGCCGCT (hg19) chrX:g.137566847C>A (hg38) chrX:g.137566847_137566853delinsAGCCGCT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.137566847C>A , CM000685.2:g.137566847C>A GRCh38
NC_000023.10:g.136649006C>A , CM000685.1:g.136649006C>A GRCh37
NC_000023.9:g.136476672C>A NCBI36
NG_008115.1:g.5661C>A
NG_008115.2:g.5721C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000287538.10:c.156C>A MANE Select ENSP00000287538.5:p.Ala52=
ENST00000287538.9:c.156C>A ENSP00000287538.5:p.Ala52=
ENST00000370606.3:c.156C>A ENSP00000359638.3:p.Ala52=
NM_003413.3:c.156C>A NP_003404.1:p.Ala52=
NM_001330661.1:c.156C>A NP_001317590.1:p.Ala52=
NM_003413.4:c.156C>A MANE Select NP_003404.1:p.Ala52=
Search 100 bp 5'
Search 100 bp 3'