Canonical Allele Identifier: CA414770753
Gene: ZIC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.136649665T>A (hg19) chrX:g.137567506T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.137567506T>A , CM000685.2:g.137567506T>A GRCh38
NC_000023.10:g.136649665T>A , CM000685.1:g.136649665T>A GRCh37
NC_000023.9:g.136477331T>A NCBI36
NG_008115.1:g.6320T>A
NG_008115.2:g.6380T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000287538.10:c.815T>A MANE Select ENSP00000287538.5:p.Phe272Tyr
ENST00000287538.9:c.815T>A ENSP00000287538.5:p.Phe272Tyr
ENST00000370606.3:c.815T>A ENSP00000359638.3:p.Phe272Tyr
NM_003413.3:c.815T>A NP_003404.1:p.Phe272Tyr
NM_001330661.1:c.815T>A NP_001317590.1:p.Phe272Tyr
NM_003413.4:c.815T>A MANE Select NP_003404.1:p.Phe272Tyr
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