Canonical Allele Identifier: CA179375824

Gene: ZFHX4

Linked Data

• dbSNP Id: rs1037013687
• gnomAD v3: 8-76864204-C-T
• gnomAD v4: 8-76864204-C-T
• MyVariant Identifiers: chr8:g.77776440C>T (hg19) ; chr8:g.76864204C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.76864204C>T , CM000670.2:g.76864204C>T	GRCh38
NC_000008.10:g.77776440C>T , CM000670.1:g.77776440C>T	GRCh37
NC_000008.9:g.77938995C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651372.2:c.10490C>T MANE Select	ENSP00000498627.1:p.Pro3497Leu
ENST00000518282.5:c.10412C>T	ENSP00000430848.1:p.Pro3471Leu
ENST00000521891.6:c.10490C>T	ENSP00000430497.2:p.Pro3497Leu
NM_024721.4:c.10490C>T	NP_078997.4:p.Pro3497Leu
XM_011517592.1:c.10490C>T	XP_011515894.1:p.Pro3497Leu
XM_011517593.1:c.10490C>T	XP_011515895.1:p.Pro3497Leu
XM_011517594.1:c.10490C>T	XP_011515896.1:p.Pro3497Leu
XM_011517595.1:c.10490C>T	XP_011515897.1:p.Pro3497Leu
XM_011517596.1:c.10412C>T	XP_011515898.1:p.Pro3471Leu
XM_011517597.1:c.10373C>T	XP_011515899.1:p.Pro3458Leu
XM_011517592.3:c.10490C>T	XP_011515894.1:p.Pro3497Leu
XM_011517593.2:c.10490C>T	XP_011515895.1:p.Pro3497Leu
XM_011517594.2:c.10490C>T	XP_011515896.1:p.Pro3497Leu
XM_011517595.2:c.10490C>T	XP_011515897.1:p.Pro3497Leu
XM_011517596.2:c.10412C>T	XP_011515898.1:p.Pro3471Leu
XM_011517597.2:c.10373C>T	XP_011515899.1:p.Pro3458Leu
XM_017013845.1:c.10295C>T	XP_016869334.1:p.Pro3432Leu
NM_024721.5:c.10490C>T MANE Select	NP_078997.4:p.Pro3497Leu