Canonical Allele Identifier: CA414770532
Gene: ZIC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.136649569T>A (hg19) chrX:g.137567410T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.137567410T>A , CM000685.2:g.137567410T>A GRCh38
NC_000023.10:g.136649569T>A , CM000685.1:g.136649569T>A GRCh37
NC_000023.9:g.136477235T>A NCBI36
NG_008115.1:g.6224T>A
NG_008115.2:g.6284T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000287538.10:c.719T>A MANE Select ENSP00000287538.5:p.Phe240Tyr
ENST00000287538.9:c.719T>A ENSP00000287538.5:p.Phe240Tyr
ENST00000370606.3:c.719T>A ENSP00000359638.3:p.Phe240Tyr
NM_003413.3:c.719T>A NP_003404.1:p.Phe240Tyr
NM_001330661.1:c.719T>A NP_001317590.1:p.Phe240Tyr
NM_003413.4:c.719T>A MANE Select NP_003404.1:p.Phe240Tyr
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