Canonical Allele Identifier: CA2722147924
Gene: ZMIZ1 HGNC NCBI

Linked Data

dbSNP Id: rs2132204195

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.79085663G>C , CM000672.2:g.79085663G>C GRCh38
NC_000010.10:g.80845420G>C , CM000672.1:g.80845420G>C GRCh37
NC_000010.9:g.80515426G>C NCBI36
NG_028289.1:g.21629G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000334512.10:c.-337+16393G>C MANE Select ENSP00000334474.5:n.-337+16393G>C
ENST00000334512.9:c.-337+16393G>C ENSP00000334474.5:n.-337+16393G>C
NM_020338.3:c.-337+16393G>C NP_065071.1:n.-337+16393G>C
XM_005269988.2:c.-337+16393G>C XP_005270045.1:n.-337+16393G>C
XM_006717923.2:c.-334+16393G>C XP_006717986.1:n.-334+16393G>C
XM_006717924.2:c.-256+16393G>C XP_006717987.1:n.-256+16393G>C
XM_006717925.2:c.-337+16393G>C XP_006717988.1:n.-337+16393G>C
XM_005269988.3:c.-337+16393G>C XP_005270045.1:n.-337+16393G>C
XM_006717923.3:c.-334+16393G>C XP_006717986.1:n.-334+16393G>C
XM_006717924.3:c.-256+16393G>C XP_006717987.1:n.-256+16393G>C
XM_006717925.3:c.-337+16393G>C XP_006717988.1:n.-337+16393G>C
NM_020338.4:c.-337+16393G>C MANE Select NP_065071.1:n.-337+16393G>C