Canonical Allele Identifier: CA2232382052
Gene: ZFHX3 HGNC NCBI

Linked Data

dbSNP Id: rs2052988514

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.73679482A>G , CM000678.2:g.73679482A>G GRCh38
NC_000016.9:g.73713381A>G , CM000678.1:g.73713381A>G GRCh37
NC_000016.8:g.72270882A>G NCBI36
NG_013211.2:g.217450T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000641206.2:c.-1547+698T>C ENSP00000493252.1:n.-1547+698T>C
ENST00000642085.1:n.163+698T>C
XR_933730.1:n.355+698T>C
XM_024450275.1:c.-494+698T>C XP_024306043.1:n.-494+698T>C
NM_001386735.1:c.-1064+698T>C NP_001373664.1:n.-1064+698T>C