Canonical Allele Identifier: CA210232341
Gene: ZCCHC24 HGNC NCBI

Linked Data

dbSNP Id: rs767827156
MyVariant Identifiers: chr10:g.81185360A>C (hg19) chr10:g.79425604A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.79425604A>C , CM000672.2:g.79425604A>C GRCh38
NC_000010.10:g.81185360A>C , CM000672.1:g.81185360A>C GRCh37
NC_000010.9:g.80855366A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000372336.4:c.447+6954T>G MANE Select ENSP00000361411.3:n.447+6954T>G
ENST00000372333.3:c.268+6954T>G ENSP00000361408.3:n.268+6954T>G
ENST00000372336.3:c.447+6954T>G ENSP00000361411.3:n.447+6954T>G
NM_153367.3:c.447+6954T>G NP_699198.2:n.447+6954T>G
XM_011539452.1:c.237+6954T>G XP_011537754.1:n.237+6954T>G
XM_011539452.3:c.237+6954T>G XP_011537754.1:n.237+6954T>G
NM_153367.4:c.447+6954T>G MANE Select NP_699198.2:n.447+6954T>G
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