Canonical Allele Identifier: CA14250635

Gene: ZFHX3

Linked Data

• dbSNP Id: rs7199343
• gnomAD v2: 16-73009024-A-T
• gnomAD v3: 16-72975125-A-T
• gnomAD v4: 16-72975125-A-T
• MyVariant Identifiers: chr16:g.73009024A>T (hg19) ; chr16:g.72975125A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.72975125A>T , CM000678.2:g.72975125A>T	GRCh38
NC_000016.9:g.73009024A>T , CM000678.1:g.73009024A>T	GRCh37
NC_000016.8:g.71566525A>T	NCBI36
NG_013211.1:g.88511T>A
NG_013211.2:g.921807T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000268489.10:c.-49-14931T>A MANE Select	ENSP00000268489.5:n.-49-14931T>A
ENST00000641206.2:c.-49-14931T>A	ENSP00000493252.1:n.-49-14931T>A
ENST00000268489.9:c.-49-14931T>A	ENSP00000268489.5:n.-49-14931T>A
ENST00000397992.5:c.-23-24160T>A	ENSP00000438926.3:n.-23-24160T>A
NM_001164766.1:c.-23-24160T>A	NP_001158238.1:n.-23-24160T>A
NM_006885.3:c.-49-14931T>A	NP_008816.3:n.-49-14931T>A
XM_005255957.2:c.-49-14931T>A	XP_005256014.1:n.-49-14931T>A
XM_005255957.4:c.-49-14931T>A	XP_005256014.1:n.-49-14931T>A
XM_017023251.2:c.71-24160T>A	XP_016878740.1:n.71-24160T>A
XM_024450291.1:c.71-24160T>A	XP_024306059.1:n.71-24160T>A
NM_006885.4:c.-49-14931T>A MANE Select	NP_008816.3:n.-49-14931T>A
NM_001164766.2:c.-23-24160T>A	NP_001158238.1:n.-23-24160T>A
NM_001386735.1:c.-49-14931T>A	NP_001373664.1:n.-49-14931T>A