Canonical Allele Identifier: CA518857782
Gene: ZIC3 HGNC NCBI

Linked Data

dbSNP Id: rs1931368084
MyVariant Identifiers: chrX:g.136649663C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.137567504C>G , CM000685.2:g.137567504C>G GRCh38
NC_000023.10:g.136649663C>G , CM000685.1:g.136649663C>G GRCh37
NC_000023.9:g.136477329C>G NCBI36
NG_008115.1:g.6318C>G
NG_008115.2:g.6378C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000287538.10:c.813C>G MANE Select ENSP00000287538.5:p.Thr271=
ENST00000287538.9:c.813C>G ENSP00000287538.5:p.Thr271=
ENST00000370606.3:c.813C>G ENSP00000359638.3:p.Thr271=
NM_003413.3:c.813C>G NP_003404.1:p.Thr271=
NM_001330661.1:c.813C>G NP_001317590.1:p.Thr271=
NM_003413.4:c.813C>G MANE Select NP_003404.1:p.Thr271=
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