Canonical Allele Identifier: CA336368798
Gene: ZIC3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1145696
ClinVar RCV Id: RCV001484648
dbSNP Id: rs1043815068
gnomAD v3: X-137567057-G-A
gnomAD v4: X-137567057-G-A
MyVariant Identifiers: chrX:g.136649216G>A (hg19) chrX:g.137567057G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.137567057G>A , CM000685.2:g.137567057G>A GRCh38
NC_000023.10:g.136649216G>A , CM000685.1:g.136649216G>A GRCh37
NC_000023.9:g.136476882G>A NCBI36
NG_008115.1:g.5871G>A
NG_008115.2:g.5931G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000287538.10:c.366G>A MANE Select ENSP00000287538.5:p.Gln122=
ENST00000287538.9:c.366G>A ENSP00000287538.5:p.Gln122=
ENST00000370606.3:c.366G>A ENSP00000359638.3:p.Gln122=
NM_003413.3:c.366G>A NP_003404.1:p.Gln122=
NM_001330661.1:c.366G>A NP_001317590.1:p.Gln122=
NM_003413.4:c.366G>A MANE Select NP_003404.1:p.Gln122=
Search 100 bp 5'
Search 100 bp 3'