Canonical Allele Identifier: CA668792221

Gene: ZMIZ1

Linked Data

• dbSNP Id: rs1250552
• gnomAD v3: 10-79298270-A-C
• gnomAD v4: 10-79298270-A-C
• MyVariant Identifiers: chr10:g.81058027A>C (hg19) ; chr10:g.79298270A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.79298270A>C , CM000672.2:g.79298270A>C	GRCh38
NC_000010.10:g.81058027A>C , CM000672.1:g.81058027A>C	GRCh37
NC_000010.9:g.80728033A>C	NCBI36
NG_028289.1:g.234236A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000334512.10:c.1492-136A>C MANE Select	ENSP00000334474.5:n.1492-136A>C
ENST00000334512.9:c.1492-136A>C	ENSP00000334474.5:n.1492-136A>C
ENST00000446377.3:c.1213-136A>C	ENSP00000401558.3:n.1213-136A>C
ENST00000611351.1:c.458+8463A>C	ENSP00000481736.1:n.458+8463A>C
NM_020338.3:c.1492-136A>C	NP_065071.1:n.1492-136A>C
XM_005269987.3:c.1510-136A>C	XP_005270044.1:n.1510-136A>C
XM_005269988.2:c.1510-136A>C	XP_005270045.1:n.1510-136A>C
XM_006717923.2:c.1510-136A>C	XP_006717986.1:n.1510-136A>C
XM_006717924.2:c.1510-136A>C	XP_006717987.1:n.1510-136A>C
XM_006717925.2:c.1510-136A>C	XP_006717988.1:n.1510-136A>C
XM_011539978.1:c.1138-136A>C	XP_011538280.1:n.1138-136A>C
XM_011539979.1:c.1138-136A>C	XP_011538281.1:n.1138-136A>C
XM_011539980.1:c.1120-136A>C	XP_011538282.1:n.1120-136A>C
XM_005269987.5:c.1510-136A>C	XP_005270044.1:n.1510-136A>C
XM_005269988.3:c.1510-136A>C	XP_005270045.1:n.1510-136A>C
XM_006717923.3:c.1510-136A>C	XP_006717986.1:n.1510-136A>C
XM_006717924.3:c.1510-136A>C	XP_006717987.1:n.1510-136A>C
XM_006717925.3:c.1510-136A>C	XP_006717988.1:n.1510-136A>C
XM_011539978.2:c.1138-136A>C	XP_011538280.1:n.1138-136A>C
XM_011539980.3:c.1120-136A>C	XP_011538282.1:n.1120-136A>C
XM_017016440.2:c.1357-136A>C	XP_016871929.1:n.1357-136A>C
XM_017016441.1:c.1138-136A>C	XP_016871930.1:n.1138-136A>C
XM_017016442.1:c.1120-136A>C	XP_016871931.1:n.1120-136A>C
XM_017016443.1:c.1138-136A>C	XP_016871932.1:n.1138-136A>C
NM_020338.4:c.1492-136A>C MANE Select	NP_065071.1:n.1492-136A>C