Canonical Allele Identifier: CA414770743
Gene: ZIC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.136649661A>C (hg19) chrX:g.137567502A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.137567502A>C , CM000685.2:g.137567502A>C GRCh38
NC_000023.10:g.136649661A>C , CM000685.1:g.136649661A>C GRCh37
NC_000023.9:g.136477327A>C NCBI36
NG_008115.1:g.6316A>C
NG_008115.2:g.6376A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000287538.10:c.811A>C MANE Select ENSP00000287538.5:p.Thr271Pro
ENST00000287538.9:c.811A>C ENSP00000287538.5:p.Thr271Pro
ENST00000370606.3:c.811A>C ENSP00000359638.3:p.Thr271Pro
NM_003413.3:c.811A>C NP_003404.1:p.Thr271Pro
NM_001330661.1:c.811A>C NP_001317590.1:p.Thr271Pro
NM_003413.4:c.811A>C MANE Select NP_003404.1:p.Thr271Pro
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