Canonical Allele Identifier: CA2232275226
Gene: ZFHX3 HGNC NCBI

Linked Data

dbSNP Id: rs2018594593

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.73467561G>A , CM000678.2:g.73467561G>A GRCh38
NC_000016.9:g.73501460G>A , CM000678.1:g.73501460G>A GRCh37
NC_000016.8:g.72058961G>A NCBI36
NG_013211.2:g.429371C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000641206.2:c.-1546-11303C>T ENSP00000493252.1:n.-1546-11303C>T
XM_024450275.1:c.-493-11303C>T XP_024306043.1:n.-493-11303C>T
NM_001386735.1:c.-1063-11303C>T NP_001373664.1:n.-1063-11303C>T