Canonical Allele Identifier: CA375975696

Gene: GATA3

Linked Data

• dbSNP Id: rs2131521372
• MyVariant Identifiers: chr10:g.8115825T>C (hg19) ; chr10:g.8073862T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8073862T>C , CM000672.2:g.8073862T>C	GRCh38
NC_000010.10:g.8115825T>C , CM000672.1:g.8115825T>C	GRCh37
NC_000010.9:g.8155831T>C	NCBI36
NG_015859.1:g.24159T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346208.4:c.1171T>C	ENSP00000341619.3:p.Phe391Leu
ENST00000379328.9:c.1174T>C MANE Select	ENSP00000368632.3:p.Phe392Leu
ENST00000346208.3:c.1171T>C	ENSP00000341619.3:p.Phe391Leu
ENST00000379328.7:c.1174T>C	ENSP00000368632.3:p.Phe392Leu
ENST00000461472.1:n.693T>C
NM_001002295.1:c.1174T>C	NP_001002295.1:p.Phe392Leu
NM_002051.2:c.1171T>C	NP_002042.1:p.Phe391Leu
XM_005252442.2:c.1174T>C	XP_005252499.1:p.Phe392Leu
XM_005252443.3:c.1174T>C	XP_005252500.1:p.Phe392Leu
XM_005252443.5:c.1174T>C	XP_005252500.1:p.Phe392Leu
NM_001002295.2:c.1174T>C MANE Select	NP_001002295.1:p.Phe392Leu
NM_002051.3:c.1171T>C	NP_002042.1:p.Phe391Leu