Canonical Allele Identifier: CA2232382077
Gene: ZFHX3 HGNC NCBI

Linked Data

dbSNP Id: rs2052989061

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.73679529C>G , CM000678.2:g.73679529C>G GRCh38
NC_000016.9:g.73713428C>G , CM000678.1:g.73713428C>G GRCh37
NC_000016.8:g.72270929C>G NCBI36
NG_013211.2:g.217403G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000641018.1:n.812G>C
ENST00000641206.2:c.-1547+651G>C ENSP00000493252.1:n.-1547+651G>C
ENST00000642085.1:n.163+651G>C
XR_933730.1:n.355+651G>C
XM_024450275.1:c.-494+651G>C XP_024306043.1:n.-494+651G>C
NM_001386735.1:c.-1064+651G>C NP_001373664.1:n.-1064+651G>C