Canonical Allele Identifier: CA2321045995

Gene: FCER2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690514T= , CM000681.2:g.7690514T=	GRCh38
NC_000019.9:g.7755400T= , CM000681.1:g.7755400T=	GRCh37
NC_000019.8:g.7661400T=	NCBI36
NG_029554.1:g.16633A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.513A= MANE Select	ENSP00000471974.1:p.Gln171=
ENST00000346664.9:c.513A=	ENSP00000264072.6:p.Gln171=
ENST00000360067.8:c.510A=	ENSP00000353178.4:p.Gln170=
ENST00000593418.1:c.450A=	ENSP00000472067.1:p.Gln150=
ENST00000597312.5:n.1038A=
ENST00000597921.5:c.513A=	ENSP00000471974.1:p.Gln171=
ENST00000597934.1:n.875A=
ENST00000598803.5:n.1008A=
NM_001207019.2:c.510A=	NP_001193948.2:p.Gln170=
NM_001220500.1:c.513A=	NP_001207429.1:p.Gln171=
NM_002002.4:c.513A=	NP_001993.2:p.Gln171=
XM_005272462.3:c.513A=	XP_005272519.1:p.Gln171=
XM_005272462.4:c.513A=	XP_005272519.1:p.Gln171=
NM_001220500.2:c.513A= MANE Select	NP_001207429.1:p.Gln171=
NM_001207019.3:c.510A=	NP_001193948.2:p.Gln170=
NM_002002.5:c.513A=	NP_001993.2:p.Gln171=