Canonical Allele Identifier: CA1146778256

Gene: FCER1G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161219150C= , CM000663.2:g.161219150C=	GRCh38
NC_000001.10:g.161188940C= , CM000663.1:g.161188940C=	GRCh37
NC_000001.9:g.159455564C=	NCBI36
NG_029043.1:g.8854C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289902.2:c.*207C= MANE Select	ENSP00000289902.1:n.*207C=
ENST00000289902.1:c.*207C=	ENSP00000289902.1:n.*207C=
ENST00000367992.7:c.198+427C=	ENSP00000356971.3:n.198+427C=
ENST00000490414.1:n.464C=
NM_004106.1:c.*207C=	NP_004097.1:n.*207C=
NM_004106.2:c.*207C= MANE Select	NP_004097.1:n.*207C=