Canonical Allele Identifier: CA668777820
Gene: ZCCHC24 HGNC NCBI

Linked Data

dbSNP Id: rs1284491453
MyVariant Identifiers: chr10:g.81185365C>T (hg19) chr10:g.79425609C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.79425609C>T , CM000672.2:g.79425609C>T GRCh38
NC_000010.10:g.81185365C>T , CM000672.1:g.81185365C>T GRCh37
NC_000010.9:g.80855371C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000372336.4:c.447+6949G>A MANE Select ENSP00000361411.3:n.447+6949G>A
ENST00000372333.3:c.268+6949G>A ENSP00000361408.3:n.268+6949G>A
ENST00000372336.3:c.447+6949G>A ENSP00000361411.3:n.447+6949G>A
NM_153367.3:c.447+6949G>A NP_699198.2:n.447+6949G>A
XM_011539452.1:c.237+6949G>A XP_011537754.1:n.237+6949G>A
XM_011539452.3:c.237+6949G>A XP_011537754.1:n.237+6949G>A
NM_153367.4:c.447+6949G>A MANE Select NP_699198.2:n.447+6949G>A
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