Canonical Allele Identifier: CA414769466
Gene: ZIC3 HGNC NCBI

Linked Data

dbSNP Id: rs1931353406
gnomAD v4: X-137566923-G-A
MyVariant Identifiers: chrX:g.136649082G>A (hg19) chrX:g.137566923G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.137566923G>A , CM000685.2:g.137566923G>A GRCh38
NC_000023.10:g.136649082G>A , CM000685.1:g.136649082G>A GRCh37
NC_000023.9:g.136476748G>A NCBI36
NG_008115.1:g.5737G>A
NG_008115.2:g.5797G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000287538.10:c.232G>A MANE Select ENSP00000287538.5:p.Gly78Ser
ENST00000287538.9:c.232G>A ENSP00000287538.5:p.Gly78Ser
ENST00000370606.3:c.232G>A ENSP00000359638.3:p.Gly78Ser
NM_003413.3:c.232G>A NP_003404.1:p.Gly78Ser
NM_001330661.1:c.232G>A NP_001317590.1:p.Gly78Ser
NM_003413.4:c.232G>A MANE Select NP_003404.1:p.Gly78Ser
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