Canonical Allele Identifier: CA2232382054
Gene: ZFHX3 HGNC NCBI

Linked Data

dbSNP Id: rs1043775658

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.73679483C>G , CM000678.2:g.73679483C>G GRCh38
NC_000016.9:g.73713382C>G , CM000678.1:g.73713382C>G GRCh37
NC_000016.8:g.72270883C>G NCBI36
NG_013211.2:g.217449G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000641206.2:c.-1547+697G>C ENSP00000493252.1:n.-1547+697G>C
ENST00000642085.1:n.163+697G>C
XR_933730.1:n.355+697G>C
XM_024450275.1:c.-494+697G>C XP_024306043.1:n.-494+697G>C
NM_001386735.1:c.-1064+697G>C NP_001373664.1:n.-1064+697G>C