Canonical Allele Identifier: CA2321049933

Gene: FCER2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7698362G= , CM000681.2:g.7698362G=	GRCh38
NC_000019.9:g.7763248G= , CM000681.1:g.7763248G=	GRCh37
NC_000019.8:g.7669248G=	NCBI36
NG_029554.1:g.8785C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.184C= MANE Select	ENSP00000471974.1:p.Arg62=
ENST00000346664.9:c.184C=	ENSP00000264072.6:p.Arg62=
ENST00000360067.8:c.181C=	ENSP00000353178.4:p.Arg61=
ENST00000593418.1:c.184C=	ENSP00000472067.1:p.Arg62=
ENST00000597312.5:n.709C=
ENST00000597921.5:c.184C=	ENSP00000471974.1:p.Arg62=
ENST00000597934.1:n.386C=
ENST00000598803.5:n.679C=
NM_001207019.2:c.181C=	NP_001193948.2:p.Arg61=
NM_001220500.1:c.184C=	NP_001207429.1:p.Arg62=
NM_002002.4:c.184C=	NP_001993.2:p.Arg62=
XM_005272462.3:c.184C=	XP_005272519.1:p.Arg62=
XM_005272462.4:c.184C=	XP_005272519.1:p.Arg62=
NM_001220500.2:c.184C= MANE Select	NP_001207429.1:p.Arg62=
NM_001207019.3:c.181C=	NP_001193948.2:p.Arg61=
NM_002002.5:c.184C=	NP_001993.2:p.Arg62=