Canonical Allele Identifier: CA468400701

Gene: GATA3

Linked Data

• dbSNP Id: rs1295805769
• gnomAD v2: 10-8115737-C-A
• MyVariant Identifiers: chr10:g.8115737C>A (hg19) ; chr10:g.8073774C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8073774C>A , CM000672.2:g.8073774C>A	GRCh38
NC_000010.10:g.8115737C>A , CM000672.1:g.8115737C>A	GRCh37
NC_000010.9:g.8155743C>A	NCBI36
NG_015859.1:g.24071C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346208.4:c.1083C>A	ENSP00000341619.3:p.Ile361=
ENST00000379328.9:c.1086C>A MANE Select	ENSP00000368632.3:p.Ile362=
ENST00000346208.3:c.1083C>A	ENSP00000341619.3:p.Ile361=
ENST00000379328.7:c.1086C>A	ENSP00000368632.3:p.Ile362=
ENST00000461472.1:n.605C>A
NM_001002295.1:c.1086C>A	NP_001002295.1:p.Ile362=
NM_002051.2:c.1083C>A	NP_002042.1:p.Ile361=
XM_005252442.2:c.1086C>A	XP_005252499.1:p.Ile362=
XM_005252443.3:c.1086C>A	XP_005252500.1:p.Ile362=
XM_005252443.5:c.1086C>A	XP_005252500.1:p.Ile362=
NM_001002295.2:c.1086C>A MANE Select	NP_001002295.1:p.Ile362=
NM_002051.3:c.1083C>A	NP_002042.1:p.Ile361=