Canonical Allele Identifier: CA10529357
Gene: ZIC3 HGNC NCBI

Linked Data

dbSNP Id: rs749500083
ExAC: X:136651031 T / C
gnomAD v2: X-136651031-T-C
gnomAD v4: X-137568872-T-C
MyVariant Identifiers: chrX:g.136651031T>C (hg19) chrX:g.137568872T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.137568872T>C , CM000685.2:g.137568872T>C GRCh38
NC_000023.10:g.136651031T>C , CM000685.1:g.136651031T>C GRCh37
NC_000023.9:g.136478697T>C NCBI36
NG_008115.1:g.7686T>C
NG_008115.2:g.7746T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000287538.10:c.1061-30T>C MANE Select ENSP00000287538.5:n.1061-30T>C
ENST00000287538.9:c.1061-30T>C ENSP00000287538.5:n.1061-30T>C
ENST00000370606.3:c.1061-30T>C ENSP00000359638.3:n.1061-30T>C
ENST00000478471.1:n.68T>C
NM_003413.3:c.1061-30T>C NP_003404.1:n.1061-30T>C
NM_001330661.1:c.1061-30T>C NP_001317590.1:n.1061-30T>C
NM_003413.4:c.1061-30T>C MANE Select NP_003404.1:n.1061-30T>C
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