Canonical Allele Identifier: CA723661317

Gene: ZFHX3

Linked Data

• dbSNP Id: rs1242385732
• gnomAD v3: 16-73679561-CAT-C
• gnomAD v4: 16-73679561-CAT-C
• MyVariant Identifiers: chr16:g.73713461_73713462del (hg19) ; chr16:g.73679562_73679563del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.73679563_73679564del , CM000678.2:g.73679563_73679564del	GRCh38
NC_000016.9:g.73713462_73713463del , CM000678.1:g.73713462_73713463del	GRCh37
NC_000016.8:g.72270963_72270964del	NCBI36
NG_013211.2:g.217369_217370del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641018.1:n.778_779del
ENST00000641206.2:c.-1547+617_-1547+618del	ENSP00000493252.1:n.-1547+617_-1547+618del
ENST00000642085.1:n.163+617_163+618del
XR_933730.1:n.355+617_355+618del
XM_024450275.1:c.-494+617_-494+618del	XP_024306043.1:n.-494+617_-494+618del
NM_001386735.1:c.-1064+617_-1064+618del	NP_001373664.1:n.-1064+617_-1064+618del