Canonical Allele Identifier: CA668777803
Gene: ZCCHC24 HGNC NCBI

Linked Data

dbSNP Id: rs1200893464
gnomAD v3: 10-79425572-A-G
gnomAD v4: 10-79425572-A-G
MyVariant Identifiers: chr10:g.81185328A>G (hg19) chr10:g.79425572A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.79425572A>G , CM000672.2:g.79425572A>G GRCh38
NC_000010.10:g.81185328A>G , CM000672.1:g.81185328A>G GRCh37
NC_000010.9:g.80855334A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000372336.4:c.447+6986T>C MANE Select ENSP00000361411.3:n.447+6986T>C
ENST00000372333.3:c.268+6986T>C ENSP00000361408.3:n.268+6986T>C
ENST00000372336.3:c.447+6986T>C ENSP00000361411.3:n.447+6986T>C
NM_153367.3:c.447+6986T>C NP_699198.2:n.447+6986T>C
XM_011539452.1:c.237+6986T>C XP_011537754.1:n.237+6986T>C
XM_011539452.3:c.237+6986T>C XP_011537754.1:n.237+6986T>C
NM_153367.4:c.447+6986T>C MANE Select NP_699198.2:n.447+6986T>C
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