Canonical Allele Identifier: CA414770175
Gene: ZIC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.136649403C>G (hg19) chrX:g.137567244C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.137567244C>G , CM000685.2:g.137567244C>G GRCh38
NC_000023.10:g.136649403C>G , CM000685.1:g.136649403C>G GRCh37
NC_000023.9:g.136477069C>G NCBI36
NG_008115.1:g.6058C>G
NG_008115.2:g.6118C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000287538.10:c.553C>G MANE Select ENSP00000287538.5:p.His185Asp
ENST00000287538.9:c.553C>G ENSP00000287538.5:p.His185Asp
ENST00000370606.3:c.553C>G ENSP00000359638.3:p.His185Asp
NM_003413.3:c.553C>G NP_003404.1:p.His185Asp
NM_001330661.1:c.553C>G NP_001317590.1:p.His185Asp
NM_003413.4:c.553C>G MANE Select NP_003404.1:p.His185Asp
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