Canonical Allele Identifier: CA414769682
Gene: ZIC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.136649176C>T (hg19) chrX:g.137567017C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.137567017C>T , CM000685.2:g.137567017C>T GRCh38
NC_000023.10:g.136649176C>T , CM000685.1:g.136649176C>T GRCh37
NC_000023.9:g.136476842C>T NCBI36
NG_008115.1:g.5831C>T
NG_008115.2:g.5891C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000287538.10:c.326C>T MANE Select ENSP00000287538.5:p.Ser109Phe
ENST00000287538.9:c.326C>T ENSP00000287538.5:p.Ser109Phe
ENST00000370606.3:c.326C>T ENSP00000359638.3:p.Ser109Phe
NM_003413.3:c.326C>T NP_003404.1:p.Ser109Phe
NM_001330661.1:c.326C>T NP_001317590.1:p.Ser109Phe
NM_003413.4:c.326C>T MANE Select NP_003404.1:p.Ser109Phe
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