Canonical Allele Identifier: CA1922019986
Gene: ZMIZ1 HGNC NCBI

Linked Data

dbSNP Id: rs1842793587

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.79085790C>G , CM000672.2:g.79085790C>G GRCh38
NC_000010.10:g.80845547C>G , CM000672.1:g.80845547C>G GRCh37
NC_000010.9:g.80515553C>G NCBI36
NG_028289.1:g.21756C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000334512.10:c.-337+16520C>G MANE Select ENSP00000334474.5:n.-337+16520C>G
ENST00000334512.9:c.-337+16520C>G ENSP00000334474.5:n.-337+16520C>G
NM_020338.3:c.-337+16520C>G NP_065071.1:n.-337+16520C>G
XM_005269988.2:c.-337+16520C>G XP_005270045.1:n.-337+16520C>G
XM_006717923.2:c.-334+16520C>G XP_006717986.1:n.-334+16520C>G
XM_006717924.2:c.-256+16520C>G XP_006717987.1:n.-256+16520C>G
XM_006717925.2:c.-337+16520C>G XP_006717988.1:n.-337+16520C>G
XM_005269988.3:c.-337+16520C>G XP_005270045.1:n.-337+16520C>G
XM_006717923.3:c.-334+16520C>G XP_006717986.1:n.-334+16520C>G
XM_006717924.3:c.-256+16520C>G XP_006717987.1:n.-256+16520C>G
XM_006717925.3:c.-337+16520C>G XP_006717988.1:n.-337+16520C>G
NM_020338.4:c.-337+16520C>G MANE Select NP_065071.1:n.-337+16520C>G