Canonical Allele Identifier: CA623477871

Gene: ZFHX3

Linked Data

• dbSNP Id: rs1302359918
• gnomAD v2: 16-73713474-CT-C
• gnomAD v3: 16-73679575-CT-C
• gnomAD v4: 16-73679575-CT-C
• MyVariant Identifiers: chr16:g.73713475del (hg19) ; chr16:g.73679576del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.73679576del , CM000678.2:g.73679576del	GRCh38
NC_000016.9:g.73713475del , CM000678.1:g.73713475del	GRCh37
NC_000016.8:g.72270976del	NCBI36
NG_013211.2:g.217356del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641018.1:n.765del
ENST00000641206.2:c.-1547+604del	ENSP00000493252.1:n.-1547+604del
ENST00000642085.1:n.163+604del
XR_933730.1:n.355+604del
XM_024450275.1:c.-494+604del	XP_024306043.1:n.-494+604del
NM_001386735.1:c.-1064+604del	NP_001373664.1:n.-1064+604del