Canonical Allele Identifier: CA1922181190

Gene: ZCCHC24

Linked Data

• dbSNP Id: rs1857016005

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.79425600T>G , CM000672.2:g.79425600T>G	GRCh38
NC_000010.10:g.81185356T>G , CM000672.1:g.81185356T>G	GRCh37
NC_000010.9:g.80855362T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372336.4:c.447+6958A>C MANE Select	ENSP00000361411.3:n.447+6958A>C
ENST00000372333.3:c.268+6958A>C	ENSP00000361408.3:n.268+6958A>C
ENST00000372336.3:c.447+6958A>C	ENSP00000361411.3:n.447+6958A>C
NM_153367.3:c.447+6958A>C	NP_699198.2:n.447+6958A>C
XM_011539452.1:c.237+6958A>C	XP_011537754.1:n.237+6958A>C
XM_011539452.3:c.237+6958A>C	XP_011537754.1:n.237+6958A>C
NM_153367.4:c.447+6958A>C MANE Select	NP_699198.2:n.447+6958A>C