Canonical Allele Identifier: CA1922075182
Gene: ZMIZ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.79200254G= , CM000672.2:g.79200254G= GRCh38
NC_000010.10:g.80960011G= , CM000672.1:g.80960011G= GRCh37
NC_000010.9:g.80630017G= NCBI36
NG_028289.1:g.136220G=

Transcript Alleles

HGVS Amino-acid change
ENST00000334512.10:c.-49-1330G= MANE Select ENSP00000334474.5:n.-49-1330G=
ENST00000334512.9:c.-49-1330G= ENSP00000334474.5:n.-49-1330G=
NM_020338.3:c.-49-1330G= NP_065071.1:n.-49-1330G=
XM_005269987.3:c.-49-1330G= XP_005270044.1:n.-49-1330G=
XM_005269988.2:c.-49-1330G= XP_005270045.1:n.-49-1330G=
XM_006717923.2:c.-49-1330G= XP_006717986.1:n.-49-1330G=
XM_006717924.2:c.-49-1330G= XP_006717987.1:n.-49-1330G=
XM_006717925.2:c.-49-1330G= XP_006717988.1:n.-49-1330G=
XM_005269987.5:c.-49-1330G= XP_005270044.1:n.-49-1330G=
XM_005269988.3:c.-49-1330G= XP_005270045.1:n.-49-1330G=
XM_006717923.3:c.-49-1330G= XP_006717986.1:n.-49-1330G=
XM_006717924.3:c.-49-1330G= XP_006717987.1:n.-49-1330G=
XM_006717925.3:c.-49-1330G= XP_006717988.1:n.-49-1330G=
NM_020338.4:c.-49-1330G= MANE Select NP_065071.1:n.-49-1330G=