Canonical Allele Identifier: CA1202650858

Gene: FCER1G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161219166A= , CM000663.2:g.161219166A=	GRCh38
NC_000001.10:g.161188956A= , CM000663.1:g.161188956A=	GRCh37
NC_000001.9:g.159455580A=	NCBI36
NG_029043.1:g.8870A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289902.2:c.*223A= MANE Select	ENSP00000289902.1:n.*223A=
ENST00000289902.1:c.*223A=	ENSP00000289902.1:n.*223A=
ENST00000367992.7:c.198+443A=	ENSP00000356971.3:n.198+443A=
ENST00000490414.1:n.480A=
NM_004106.1:c.*223A=	NP_004097.1:n.*223A=
NM_004106.2:c.*223A= MANE Select	NP_004097.1:n.*223A=