Canonical Allele Identifier: CA2232382074
Gene: ZFHX3 HGNC NCBI

Linked Data

dbSNP Id: rs2052988999

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.73679526T>G , CM000678.2:g.73679526T>G GRCh38
NC_000016.9:g.73713425T>G , CM000678.1:g.73713425T>G GRCh37
NC_000016.8:g.72270926T>G NCBI36
NG_013211.2:g.217406A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000641018.1:n.815A>C
ENST00000641206.2:c.-1547+654A>C ENSP00000493252.1:n.-1547+654A>C
ENST00000642085.1:n.163+654A>C
XR_933730.1:n.355+654A>C
XM_024450275.1:c.-494+654A>C XP_024306043.1:n.-494+654A>C
NM_001386735.1:c.-1064+654A>C NP_001373664.1:n.-1064+654A>C