Canonical Allele Identifier: CA668753163

Gene: ZMIZ1

Linked Data

• dbSNP Id: rs1250009
• MyVariant Identifiers: chr10:g.80845411G>C (hg19) ; chr10:g.79085654G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.79085654G>C , CM000672.2:g.79085654G>C	GRCh38
NC_000010.10:g.80845411G>C , CM000672.1:g.80845411G>C	GRCh37
NC_000010.9:g.80515417G>C	NCBI36
NG_028289.1:g.21620G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000334512.10:c.-337+16384G>C MANE Select	ENSP00000334474.5:n.-337+16384G>C
ENST00000334512.9:c.-337+16384G>C	ENSP00000334474.5:n.-337+16384G>C
NM_020338.3:c.-337+16384G>C	NP_065071.1:n.-337+16384G>C
XM_005269988.2:c.-337+16384G>C	XP_005270045.1:n.-337+16384G>C
XM_006717923.2:c.-334+16384G>C	XP_006717986.1:n.-334+16384G>C
XM_006717924.2:c.-256+16384G>C	XP_006717987.1:n.-256+16384G>C
XM_006717925.2:c.-337+16384G>C	XP_006717988.1:n.-337+16384G>C
XM_005269988.3:c.-337+16384G>C	XP_005270045.1:n.-337+16384G>C
XM_006717923.3:c.-334+16384G>C	XP_006717986.1:n.-334+16384G>C
XM_006717924.3:c.-256+16384G>C	XP_006717987.1:n.-256+16384G>C
XM_006717925.3:c.-337+16384G>C	XP_006717988.1:n.-337+16384G>C
NM_020338.4:c.-337+16384G>C MANE Select	NP_065071.1:n.-337+16384G>C