Canonical Allele Identifier: CA210232344
Gene: ZCCHC24 HGNC NCBI

Linked Data

dbSNP Id: rs1038251948
MyVariant Identifiers: chr10:g.81185368G>A (hg19) chr10:g.79425612G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.79425612G>A , CM000672.2:g.79425612G>A GRCh38
NC_000010.10:g.81185368G>A , CM000672.1:g.81185368G>A GRCh37
NC_000010.9:g.80855374G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000372336.4:c.447+6946C>T MANE Select ENSP00000361411.3:n.447+6946C>T
ENST00000372333.3:c.268+6946C>T ENSP00000361408.3:n.268+6946C>T
ENST00000372336.3:c.447+6946C>T ENSP00000361411.3:n.447+6946C>T
NM_153367.3:c.447+6946C>T NP_699198.2:n.447+6946C>T
XM_011539452.1:c.237+6946C>T XP_011537754.1:n.237+6946C>T
XM_011539452.3:c.237+6946C>T XP_011537754.1:n.237+6946C>T
NM_153367.4:c.447+6946C>T MANE Select NP_699198.2:n.447+6946C>T
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