Canonical Allele Identifier: CA2321045831

Gene: FCER2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690206G= , CM000681.2:g.7690206G=	GRCh38
NC_000019.9:g.7755092G= , CM000681.1:g.7755092G=	GRCh37
NC_000019.8:g.7661092G=	NCBI36
NG_029554.1:g.16941C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.681C= MANE Select	ENSP00000471974.1:p.Asp227=
ENST00000346664.9:c.681C=	ENSP00000264072.6:p.Asp227=
ENST00000360067.8:c.678C=	ENSP00000353178.4:p.Asp226=
ENST00000597312.5:n.1206C=
ENST00000597921.5:c.681C=	ENSP00000471974.1:p.Asp227=
ENST00000597934.1:n.1043C=
ENST00000598803.5:n.1176C=
NM_001207019.2:c.678C=	NP_001193948.2:p.Asp226=
NM_001220500.1:c.681C=	NP_001207429.1:p.Asp227=
NM_002002.4:c.681C=	NP_001993.2:p.Asp227=
XM_005272462.3:c.681C=	XP_005272519.1:p.Asp227=
XM_005272462.4:c.681C=	XP_005272519.1:p.Asp227=
NM_001220500.2:c.681C= MANE Select	NP_001207429.1:p.Asp227=
NM_001207019.3:c.678C=	NP_001193948.2:p.Asp226=
NM_002002.5:c.681C=	NP_001993.2:p.Asp227=