Canonical Allele Identifier: CA210232337

Gene: ZCCHC24

Linked Data

• dbSNP Id: rs951906998
• MyVariant Identifiers: chr10:g.81185332G>C (hg19) ; chr10:g.79425576G>C (hg38)

Genomic Alleles

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

Transcript Alleles

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