Canonical Allele Identifier: CA1922181180
Gene: ZCCHC24 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.79425576G= , CM000672.2:g.79425576G= GRCh38
NC_000010.10:g.81185332G= , CM000672.1:g.81185332G= GRCh37
NC_000010.9:g.80855338G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000372336.4:c.447+6982C= MANE Select ENSP00000361411.3:n.447+6982C=
ENST00000372333.3:c.268+6982C= ENSP00000361408.3:n.268+6982C=
ENST00000372336.3:c.447+6982C= ENSP00000361411.3:n.447+6982C=
NM_153367.3:c.447+6982C= NP_699198.2:n.447+6982C=
XM_011539452.1:c.237+6982C= XP_011537754.1:n.237+6982C=
XM_011539452.3:c.237+6982C= XP_011537754.1:n.237+6982C=
NM_153367.4:c.447+6982C= MANE Select NP_699198.2:n.447+6982C=
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