Canonical Allele Identifier: CA414771469
Gene: ZIC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.136651113C>A (hg19) chrX:g.137568954C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.137568954C>A , CM000685.2:g.137568954C>A GRCh38
NC_000023.10:g.136651113C>A , CM000685.1:g.136651113C>A GRCh37
NC_000023.9:g.136478779C>A NCBI36
NG_008115.1:g.7768C>A
NG_008115.2:g.7828C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000287538.10:c.1113C>A MANE Select ENSP00000287538.5:p.Asn371Lys
ENST00000287538.9:c.1113C>A ENSP00000287538.5:p.Asn371Lys
ENST00000370606.3:c.1113C>A ENSP00000359638.3:p.Asn371Lys
ENST00000478471.1:n.150C>A
NM_003413.3:c.1113C>A NP_003404.1:p.Asn371Lys
NM_001330661.1:c.1113C>A NP_001317590.1:p.Asn371Lys
NM_003413.4:c.1113C>A MANE Select NP_003404.1:p.Asn371Lys
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