Canonical Allele Identifier: CA179375851

Gene: ZFHX4

Linked Data

• ClinVar Variation Id: 799764
• ClinVar RCV Id: RCV000983383
• dbSNP Id: rs144584925
• gnomAD v2: 8-77776486-T-C
• gnomAD v3: 8-76864250-T-C
• gnomAD v4: 8-76864250-T-C
• MyVariant Identifiers: chr8:g.77776486T>C (hg19) ; chr8:g.76864250T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.76864250T>C , CM000670.2:g.76864250T>C	GRCh38
NC_000008.10:g.77776486T>C , CM000670.1:g.77776486T>C	GRCh37
NC_000008.9:g.77939041T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651372.2:c.10536T>C MANE Select	ENSP00000498627.1:p.Asn3512=
ENST00000518282.5:c.10458T>C	ENSP00000430848.1:p.Asn3486=
ENST00000521891.6:c.10536T>C	ENSP00000430497.2:p.Asn3512=
NM_024721.4:c.10536T>C	NP_078997.4:p.Asn3512=
XM_011517592.1:c.10536T>C	XP_011515894.1:p.Asn3512=
XM_011517593.1:c.10536T>C	XP_011515895.1:p.Asn3512=
XM_011517594.1:c.10536T>C	XP_011515896.1:p.Asn3512=
XM_011517595.1:c.10536T>C	XP_011515897.1:p.Asn3512=
XM_011517596.1:c.10458T>C	XP_011515898.1:p.Asn3486=
XM_011517597.1:c.10419T>C	XP_011515899.1:p.Asn3473=
XM_011517592.3:c.10536T>C	XP_011515894.1:p.Asn3512=
XM_011517593.2:c.10536T>C	XP_011515895.1:p.Asn3512=
XM_011517594.2:c.10536T>C	XP_011515896.1:p.Asn3512=
XM_011517595.2:c.10536T>C	XP_011515897.1:p.Asn3512=
XM_011517596.2:c.10458T>C	XP_011515898.1:p.Asn3486=
XM_011517597.2:c.10419T>C	XP_011515899.1:p.Asn3473=
XM_017013845.1:c.10341T>C	XP_016869334.1:p.Asn3447=
NM_024721.5:c.10536T>C MANE Select	NP_078997.4:p.Asn3512=