Canonical Allele Identifier: CA414769299
Gene: ZIC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.136649005C>A (hg19) chrX:g.137566846C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.137566846C>A , CM000685.2:g.137566846C>A GRCh38
NC_000023.10:g.136649005C>A , CM000685.1:g.136649005C>A GRCh37
NC_000023.9:g.136476671C>A NCBI36
NG_008115.1:g.5660C>A
NG_008115.2:g.5720C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000287538.10:c.155C>A MANE Select ENSP00000287538.5:p.Ala52Asp
ENST00000287538.9:c.155C>A ENSP00000287538.5:p.Ala52Asp
ENST00000370606.3:c.155C>A ENSP00000359638.3:p.Ala52Asp
NM_003413.3:c.155C>A NP_003404.1:p.Ala52Asp
NM_001330661.1:c.155C>A NP_001317590.1:p.Ala52Asp
NM_003413.4:c.155C>A MANE Select NP_003404.1:p.Ala52Asp
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