Canonical Allele Identifier: CA281603
Gene: ZIC3 HGNC NCBI

Linked Data

ClinVar Variation Id: 11434
ClinVar RCV Id: RCV000012187
dbSNP Id: rs122462166
MyVariant Identifiers: chrX:g.136649654C>A (hg19) chrX:g.137567495C>A (hg38)
PubMed: PMID:9354794
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.137567495C>A , CM000685.2:g.137567495C>A GRCh38
NC_000023.10:g.136649654C>A , CM000685.1:g.136649654C>A GRCh37
NC_000023.9:g.136477320C>A NCBI36
NG_008115.1:g.6309C>A
NG_008115.2:g.6369C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000287538.10:c.804C>A MANE Select ENSP00000287538.5:p.Cys268Ter
ENST00000287538.9:c.804C>A ENSP00000287538.5:p.Cys268Ter
ENST00000370606.3:c.804C>A ENSP00000359638.3:p.Cys268Ter
NM_003413.3:c.804C>A NP_003404.1:p.Cys268Ter
NM_001330661.1:c.804C>A NP_001317590.1:p.Cys268Ter
NM_003413.4:c.804C>A MANE Select NP_003404.1:p.Cys268Ter
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