Canonical Allele Identifier: CA2232382282
Gene: ZFHX3 HGNC NCBI

Linked Data

dbSNP Id: rs2052993271

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.73679930C>T , CM000678.2:g.73679930C>T GRCh38
NC_000016.9:g.73713829C>T , CM000678.1:g.73713829C>T GRCh37
NC_000016.8:g.72271330C>T NCBI36
NG_013211.2:g.217002G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000641018.1:n.411G>A
ENST00000641206.2:c.-1547+250G>A ENSP00000493252.1:n.-1547+250G>A
ENST00000642085.1:n.163+250G>A
XR_933730.1:n.355+250G>A
XM_024450275.1:c.-494+250G>A XP_024306043.1:n.-494+250G>A
NM_001386735.1:c.-1064+250G>A NP_001373664.1:n.-1064+250G>A