Canonical Allele Identifier: CA10529337
Gene: ZIC3 HGNC NCBI

Linked Data

dbSNP Id: rs769915486
ExAC: X:136649806 T / C
gnomAD v2: X-136649806-T-C
MyVariant Identifiers: chrX:g.136649806T>C (hg19) chrX:g.137567647T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.137567647T>C , CM000685.2:g.137567647T>C GRCh38
NC_000023.10:g.136649806T>C , CM000685.1:g.136649806T>C GRCh37
NC_000023.9:g.136477472T>C NCBI36
NG_008115.1:g.6461T>C
NG_008115.2:g.6521T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000287538.10:c.956T>C MANE Select ENSP00000287538.5:p.Ile319Thr
ENST00000287538.9:c.956T>C ENSP00000287538.5:p.Ile319Thr
ENST00000370606.3:c.956T>C ENSP00000359638.3:p.Ile319Thr
NM_003413.3:c.956T>C NP_003404.1:p.Ile319Thr
NM_001330661.1:c.956T>C NP_001317590.1:p.Ile319Thr
NM_003413.4:c.956T>C MANE Select NP_003404.1:p.Ile319Thr
Search 100 bp 5'
Search 100 bp 3'