Canonical Allele Identifier: CA468400627

Gene: GATA3

Linked Data

• MyVariant Identifiers: chr10:g.8097855C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8055892C>T , CM000672.2:g.8055892C>T	GRCh38
NC_000010.10:g.8097855C>T , CM000672.1:g.8097855C>T	GRCh37
NC_000010.9:g.8137861C>T	NCBI36
NG_015859.1:g.6189C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346208.4:c.237C>T	ENSP00000341619.3:p.His79=
ENST00000379328.9:c.237C>T MANE Select	ENSP00000368632.3:p.His79=
ENST00000481743.2:c.237C>T	ENSP00000493486.1:p.His79=
ENST00000643001.1:c.237C>T	ENSP00000494284.1:p.His79=
ENST00000346208.3:c.237C>T	ENSP00000341619.3:p.His79=
ENST00000379328.7:c.237C>T	ENSP00000368632.3:p.His79=
NM_001002295.1:c.237C>T	NP_001002295.1:p.His79=
NM_002051.2:c.237C>T	NP_002042.1:p.His79=
XM_005252442.2:c.237C>T	XP_005252499.1:p.His79=
XM_005252443.3:c.237C>T	XP_005252500.1:p.His79=
XM_005252443.5:c.237C>T	XP_005252500.1:p.His79=
XR_001747358.1:n.617+874G>A
NM_001002295.2:c.237C>T MANE Select	NP_001002295.1:p.His79=
NM_002051.3:c.237C>T	NP_002042.1:p.His79=