Canonical Allele Identifier: CA2232382069
Gene: ZFHX3 HGNC NCBI

Linked Data

dbSNP Id: rs2052988874

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.73679514T>A , CM000678.2:g.73679514T>A GRCh38
NC_000016.9:g.73713413T>A , CM000678.1:g.73713413T>A GRCh37
NC_000016.8:g.72270914T>A NCBI36
NG_013211.2:g.217418A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000641018.1:n.827A>T
ENST00000641206.2:c.-1547+666A>T ENSP00000493252.1:n.-1547+666A>T
ENST00000642085.1:n.163+666A>T
XR_933730.1:n.355+666A>T
XM_024450275.1:c.-494+666A>T XP_024306043.1:n.-494+666A>T
NM_001386735.1:c.-1064+666A>T NP_001373664.1:n.-1064+666A>T