Canonical Allele Identifier: CA13161407

Gene: ZMIZ1

Linked Data

• dbSNP Id: rs780151
• gnomAD v2: 10-80931481-G-A
• gnomAD v3: 10-79171724-G-A
• gnomAD v4: 10-79171724-G-A
• MyVariant Identifiers: chr10:g.80931481G>A (hg19) ; chr10:g.79171724G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.79171724G>A , CM000672.2:g.79171724G>A	GRCh38
NC_000010.10:g.80931481G>A , CM000672.1:g.80931481G>A	GRCh37
NC_000010.9:g.80601487G>A	NCBI36
NG_028289.1:g.107690G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000334512.10:c.-50+9591G>A MANE Select	ENSP00000334474.5:n.-50+9591G>A
ENST00000334512.9:c.-50+9591G>A	ENSP00000334474.5:n.-50+9591G>A
NM_020338.3:c.-50+9591G>A	NP_065071.1:n.-50+9591G>A
XM_005269987.3:c.-50+9591G>A	XP_005270044.1:n.-50+9591G>A
XM_005269988.2:c.-50+9591G>A	XP_005270045.1:n.-50+9591G>A
XM_006717923.2:c.-50+9591G>A	XP_006717986.1:n.-50+9591G>A
XM_006717924.2:c.-49-29860G>A	XP_006717987.1:n.-49-29860G>A
XM_006717925.2:c.-50+9591G>A	XP_006717988.1:n.-50+9591G>A
XM_005269987.5:c.-50+9591G>A	XP_005270044.1:n.-50+9591G>A
XM_005269988.3:c.-50+9591G>A	XP_005270045.1:n.-50+9591G>A
XM_006717923.3:c.-50+9591G>A	XP_006717986.1:n.-50+9591G>A
XM_006717924.3:c.-49-29860G>A	XP_006717987.1:n.-49-29860G>A
XM_006717925.3:c.-50+9591G>A	XP_006717988.1:n.-50+9591G>A
NM_020338.4:c.-50+9591G>A MANE Select	NP_065071.1:n.-50+9591G>A