Canonical Allele Identifier: CA403109115

Gene: FCER2

Linked Data

• MyVariant Identifiers: chr19:g.7755384A>T (hg19) ; chr19:g.7690498A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690498A>T , CM000681.2:g.7690498A>T	GRCh38
NC_000019.9:g.7755384A>T , CM000681.1:g.7755384A>T	GRCh37
NC_000019.8:g.7661384A>T	NCBI36
NG_029554.1:g.16649T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.529T>A MANE Select	ENSP00000471974.1:p.Phe177Ile
ENST00000346664.9:c.529T>A	ENSP00000264072.6:p.Phe177Ile
ENST00000360067.8:c.526T>A	ENSP00000353178.4:p.Phe176Ile
ENST00000593418.1:c.466T>A	ENSP00000472067.1:p.Phe156Ile
ENST00000597312.5:n.1054T>A
ENST00000597921.5:c.529T>A	ENSP00000471974.1:p.Phe177Ile
ENST00000597934.1:n.891T>A
ENST00000598803.5:n.1024T>A
NM_001207019.2:c.526T>A	NP_001193948.2:p.Phe176Ile
NM_001220500.1:c.529T>A	NP_001207429.1:p.Phe177Ile
NM_002002.4:c.529T>A	NP_001993.2:p.Phe177Ile
XM_005272462.3:c.529T>A	XP_005272519.1:p.Phe177Ile
XM_005272462.4:c.529T>A	XP_005272519.1:p.Phe177Ile
NM_001220500.2:c.529T>A MANE Select	NP_001207429.1:p.Phe177Ile
NM_001207019.3:c.526T>A	NP_001193948.2:p.Phe176Ile
NM_002002.5:c.529T>A	NP_001993.2:p.Phe177Ile