Canonical Allele Identifier: CA284007731
Gene: ZFHX3 HGNC NCBI

Linked Data

dbSNP Id: rs78025721
gnomAD v2: 16-73713576-T-C
gnomAD v3: 16-73679677-T-C
gnomAD v4: 16-73679677-T-C
MyVariant Identifiers: chr16:g.73713576T>C (hg19) chr16:g.73679677T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.73679677T>C , CM000678.2:g.73679677T>C GRCh38
NC_000016.9:g.73713576T>C , CM000678.1:g.73713576T>C GRCh37
NC_000016.8:g.72271077T>C NCBI36
NG_013211.2:g.217255A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000641018.1:n.664A>G
ENST00000641206.2:c.-1547+503A>G ENSP00000493252.1:n.-1547+503A>G
ENST00000642085.1:n.163+503A>G
XR_933730.1:n.355+503A>G
XM_024450275.1:c.-494+503A>G XP_024306043.1:n.-494+503A>G
NM_001386735.1:c.-1064+503A>G NP_001373664.1:n.-1064+503A>G
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