Canonical Allele Identifier: CA518857560
Gene: ZIC3 HGNC NCBI

Linked Data

gnomAD v4: X-137567048-G-C
MyVariant Identifiers: chrX:g.136649207G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.137567048G>C , CM000685.2:g.137567048G>C GRCh38
NC_000023.10:g.136649207G>C , CM000685.1:g.136649207G>C GRCh37
NC_000023.9:g.136476873G>C NCBI36
NG_008115.1:g.5862G>C
NG_008115.2:g.5922G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000287538.10:c.357G>C MANE Select ENSP00000287538.5:p.Leu119=
ENST00000287538.9:c.357G>C ENSP00000287538.5:p.Leu119=
ENST00000370606.3:c.357G>C ENSP00000359638.3:p.Leu119=
NM_003413.3:c.357G>C NP_003404.1:p.Leu119=
NM_001330661.1:c.357G>C NP_001317590.1:p.Leu119=
NM_003413.4:c.357G>C MANE Select NP_003404.1:p.Leu119=
Search 100 bp 5'
Search 100 bp 3'