Canonical Allele Identifier: CA414771484
Gene: ZIC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.136651118G>C (hg19) chrX:g.137568959G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.137568959G>C , CM000685.2:g.137568959G>C GRCh38
NC_000023.10:g.136651118G>C , CM000685.1:g.136651118G>C GRCh37
NC_000023.9:g.136478784G>C NCBI36
NG_008115.1:g.7773G>C
NG_008115.2:g.7833G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000287538.10:c.1118G>C MANE Select ENSP00000287538.5:p.Ser373Thr
ENST00000287538.9:c.1118G>C ENSP00000287538.5:p.Ser373Thr
ENST00000370606.3:c.1118G>C ENSP00000359638.3:p.Ser373Thr
ENST00000478471.1:n.155G>C
NM_003413.3:c.1118G>C NP_003404.1:p.Ser373Thr
NM_001330661.1:c.1118G>C NP_001317590.1:p.Ser373Thr
NM_003413.4:c.1118G>C MANE Select NP_003404.1:p.Ser373Thr
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