Canonical Allele Identifier: CA2321046008

Gene: FCER2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690542G= , CM000681.2:g.7690542G=	GRCh38
NC_000019.9:g.7755428G= , CM000681.1:g.7755428G=	GRCh37
NC_000019.8:g.7661428G=	NCBI36
NG_029554.1:g.16605C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.485C= MANE Select	ENSP00000471974.1:p.Thr162=
ENST00000346664.9:c.485C=	ENSP00000264072.6:p.Thr162=
ENST00000360067.8:c.482C=	ENSP00000353178.4:p.Thr161=
ENST00000593418.1:c.422C=	ENSP00000472067.1:p.Thr141=
ENST00000597312.5:n.1010C=
ENST00000597921.5:c.485C=	ENSP00000471974.1:p.Thr162=
ENST00000597934.1:n.847C=
ENST00000598803.5:n.980C=
NM_001207019.2:c.482C=	NP_001193948.2:p.Thr161=
NM_001220500.1:c.485C=	NP_001207429.1:p.Thr162=
NM_002002.4:c.485C=	NP_001993.2:p.Thr162=
XM_005272462.3:c.485C=	XP_005272519.1:p.Thr162=
XM_005272462.4:c.485C=	XP_005272519.1:p.Thr162=
NM_001220500.2:c.485C= MANE Select	NP_001207429.1:p.Thr162=
NM_001207019.3:c.482C=	NP_001193948.2:p.Thr161=
NM_002002.5:c.485C=	NP_001993.2:p.Thr162=