Canonical Allele Identifier: CA414769377
Gene: ZIC3 HGNC NCBI

Linked Data

dbSNP Id: rs1210045566
gnomAD v3: X-137566883-C-G
gnomAD v4: X-137566883-C-G
MyVariant Identifiers: chrX:g.136649042C>G (hg19) chrX:g.137566883C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.137566883C>G , CM000685.2:g.137566883C>G GRCh38
NC_000023.10:g.136649042C>G , CM000685.1:g.136649042C>G GRCh37
NC_000023.9:g.136476708C>G NCBI36
NG_008115.1:g.5697C>G
NG_008115.2:g.5757C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000287538.10:c.192C>G MANE Select ENSP00000287538.5:p.His64Gln
ENST00000287538.9:c.192C>G ENSP00000287538.5:p.His64Gln
ENST00000370606.3:c.192C>G ENSP00000359638.3:p.His64Gln
NM_003413.3:c.192C>G NP_003404.1:p.His64Gln
NM_001330661.1:c.192C>G NP_001317590.1:p.His64Gln
NM_003413.4:c.192C>G MANE Select NP_003404.1:p.His64Gln
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