Canonical Allele Identifier: CA468400399

Gene: GATA3

Linked Data

• gnomAD v4: 10-8055799-T-C
• MyVariant Identifiers: chr10:g.8097762T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8055799T>C , CM000672.2:g.8055799T>C	GRCh38
NC_000010.10:g.8097762T>C , CM000672.1:g.8097762T>C	GRCh37
NC_000010.9:g.8137768T>C	NCBI36
NG_015859.1:g.6096T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346208.4:c.144T>C	ENSP00000341619.3:p.Asp48=
ENST00000379328.9:c.144T>C MANE Select	ENSP00000368632.3:p.Asp48=
ENST00000481743.2:c.144T>C	ENSP00000493486.1:p.Asp48=
ENST00000643001.1:c.144T>C	ENSP00000494284.1:p.Asp48=
ENST00000346208.3:c.144T>C	ENSP00000341619.3:p.Asp48=
ENST00000379328.7:c.144T>C	ENSP00000368632.3:p.Asp48=
NM_001002295.1:c.144T>C	NP_001002295.1:p.Asp48=
NM_002051.2:c.144T>C	NP_002042.1:p.Asp48=
XM_005252442.2:c.144T>C	XP_005252499.1:p.Asp48=
XM_005252443.3:c.144T>C	XP_005252500.1:p.Asp48=
XM_005252443.5:c.144T>C	XP_005252500.1:p.Asp48=
XR_001747358.1:n.617+967A>G
NM_001002295.2:c.144T>C MANE Select	NP_001002295.1:p.Asp48=
NM_002051.3:c.144T>C	NP_002042.1:p.Asp48=