Canonical Allele Identifier: CA1142643002

Gene: FCER1G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161219135T= , CM000663.2:g.161219135T=	GRCh38
NC_000001.10:g.161188925T= , CM000663.1:g.161188925T=	GRCh37
NC_000001.9:g.159455549T=	NCBI36
NG_029043.1:g.8839T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289902.2:c.*192T= MANE Select	ENSP00000289902.1:n.*192T=
ENST00000289902.1:c.*192T=	ENSP00000289902.1:n.*192T=
ENST00000367992.7:c.198+412T=	ENSP00000356971.3:n.198+412T=
ENST00000490414.1:n.449T=
NM_004106.1:c.*192T=	NP_004097.1:n.*192T=
NM_004106.2:c.*192T= MANE Select	NP_004097.1:n.*192T=