Canonical Allele Identifier: CA414769608
Gene: ZIC3 HGNC NCBI

Linked Data

dbSNP Id: rs1174562828
gnomAD v2: X-136649142-A-T
gnomAD v4: X-137566983-A-T
MyVariant Identifiers: chrX:g.136649142A>T (hg19) chrX:g.137566983A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.137566983A>T , CM000685.2:g.137566983A>T GRCh38
NC_000023.10:g.136649142A>T , CM000685.1:g.136649142A>T GRCh37
NC_000023.9:g.136476808A>T NCBI36
NG_008115.1:g.5797A>T
NG_008115.2:g.5857A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000287538.10:c.292A>T MANE Select ENSP00000287538.5:p.Thr98Ser
ENST00000287538.9:c.292A>T ENSP00000287538.5:p.Thr98Ser
ENST00000370606.3:c.292A>T ENSP00000359638.3:p.Thr98Ser
NM_003413.3:c.292A>T NP_003404.1:p.Thr98Ser
NM_001330661.1:c.292A>T NP_001317590.1:p.Thr98Ser
NM_003413.4:c.292A>T MANE Select NP_003404.1:p.Thr98Ser
Search 100 bp 5'
Search 100 bp 3'