Canonical Allele Identifier: CA414771716

Gene: ZIC3

Linked Data

• MyVariant Identifiers: chrX:g.136651216C>G (hg19) ; chrX:g.137569057C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.137569057C>G , CM000685.2:g.137569057C>G	GRCh38
NC_000023.10:g.136651216C>G , CM000685.1:g.136651216C>G	GRCh37
NC_000023.9:g.136478882C>G	NCBI36
NG_008115.1:g.7871C>G
NG_008115.2:g.7931C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000287538.10:c.1216C>G MANE Select	ENSP00000287538.5:p.His406Asp
ENST00000287538.9:c.1216C>G	ENSP00000287538.5:p.His406Asp
ENST00000370606.3:c.1216C>G	ENSP00000359638.3:p.His406Asp
ENST00000478471.1:n.253C>G
NM_003413.3:c.1216C>G	NP_003404.1:p.His406Asp
NM_001330661.1:c.1216C>G	NP_001317590.1:p.His406Asp
NM_003413.4:c.1216C>G MANE Select	NP_003404.1:p.His406Asp