Canonical Allele Identifier: CA1922019914
Gene: ZMIZ1 HGNC NCBI

Linked Data

dbSNP Id: rs1250009

Genomic Alleles

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

Transcript Alleles

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