Canonical Allele Identifier: CA403106919

Gene: FCER2

Linked Data

• MyVariant Identifiers: chr19:g.7755096A>T (hg19) ; chr19:g.7690210A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690210A>T , CM000681.2:g.7690210A>T	GRCh38
NC_000019.9:g.7755096A>T , CM000681.1:g.7755096A>T	GRCh37
NC_000019.8:g.7661096A>T	NCBI36
NG_029554.1:g.16937T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.677T>A MANE Select	ENSP00000471974.1:p.Leu226Ter
ENST00000346664.9:c.677T>A	ENSP00000264072.6:p.Leu226Ter
ENST00000360067.8:c.674T>A	ENSP00000353178.4:p.Leu225Ter
ENST00000597312.5:n.1202T>A
ENST00000597921.5:c.677T>A	ENSP00000471974.1:p.Leu226Ter
ENST00000597934.1:n.1039T>A
ENST00000598803.5:n.1172T>A
NM_001207019.2:c.674T>A	NP_001193948.2:p.Leu225Ter
NM_001220500.1:c.677T>A	NP_001207429.1:p.Leu226Ter
NM_002002.4:c.677T>A	NP_001993.2:p.Leu226Ter
XM_005272462.3:c.677T>A	XP_005272519.1:p.Leu226Ter
XM_005272462.4:c.677T>A	XP_005272519.1:p.Leu226Ter
NM_001220500.2:c.677T>A MANE Select	NP_001207429.1:p.Leu226Ter
NM_001207019.3:c.674T>A	NP_001193948.2:p.Leu225Ter
NM_002002.5:c.677T>A	NP_001993.2:p.Leu226Ter