Canonical Allele Identifier: CA518857871
Gene: ZIC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.136649822C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.137567663C>T , CM000685.2:g.137567663C>T GRCh38
NC_000023.10:g.136649822C>T , CM000685.1:g.136649822C>T GRCh37
NC_000023.9:g.136477488C>T NCBI36
NG_008115.1:g.6477C>T
NG_008115.2:g.6537C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000287538.10:c.972C>T MANE Select ENSP00000287538.5:p.Gly324=
ENST00000287538.9:c.972C>T ENSP00000287538.5:p.Gly324=
ENST00000370606.3:c.972C>T ENSP00000359638.3:p.Gly324=
NM_003413.3:c.972C>T NP_003404.1:p.Gly324=
NM_001330661.1:c.972C>T NP_001317590.1:p.Gly324=
NM_003413.4:c.972C>T MANE Select NP_003404.1:p.Gly324=