Canonical Allele Identifier: CA594668502

Gene: ZMIZ1

Linked Data

• dbSNP Id: rs1333964008
• gnomAD v2: 10-80845432-C-G
• gnomAD v3: 10-79085675-C-G
• gnomAD v4: 10-79085675-C-G
• MyVariant Identifiers: chr10:g.80845432C>G (hg19) ; chr10:g.79085675C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.79085675C>G , CM000672.2:g.79085675C>G	GRCh38
NC_000010.10:g.80845432C>G , CM000672.1:g.80845432C>G	GRCh37
NC_000010.9:g.80515438C>G	NCBI36
NG_028289.1:g.21641C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334512.10:c.-337+16405C>G MANE Select	ENSP00000334474.5:n.-337+16405C>G
ENST00000334512.9:c.-337+16405C>G	ENSP00000334474.5:n.-337+16405C>G
NM_020338.3:c.-337+16405C>G	NP_065071.1:n.-337+16405C>G
XM_005269988.2:c.-337+16405C>G	XP_005270045.1:n.-337+16405C>G
XM_006717923.2:c.-334+16405C>G	XP_006717986.1:n.-334+16405C>G
XM_006717924.2:c.-256+16405C>G	XP_006717987.1:n.-256+16405C>G
XM_006717925.2:c.-337+16405C>G	XP_006717988.1:n.-337+16405C>G
XM_005269988.3:c.-337+16405C>G	XP_005270045.1:n.-337+16405C>G
XM_006717923.3:c.-334+16405C>G	XP_006717986.1:n.-334+16405C>G
XM_006717924.3:c.-256+16405C>G	XP_006717987.1:n.-256+16405C>G
XM_006717925.3:c.-337+16405C>G	XP_006717988.1:n.-337+16405C>G
NM_020338.4:c.-337+16405C>G MANE Select	NP_065071.1:n.-337+16405C>G