Canonical Allele Identifier: CA1202650854

Gene: FCER1G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161219157T= , CM000663.2:g.161219157T=	GRCh38
NC_000001.10:g.161188947T= , CM000663.1:g.161188947T=	GRCh37
NC_000001.9:g.159455571T=	NCBI36
NG_029043.1:g.8861T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289902.2:c.*214T= MANE Select	ENSP00000289902.1:n.*214T=
ENST00000289902.1:c.*214T=	ENSP00000289902.1:n.*214T=
ENST00000367992.7:c.198+434T=	ENSP00000356971.3:n.198+434T=
ENST00000490414.1:n.471T=
NM_004106.1:c.*214T=	NP_004097.1:n.*214T=
NM_004106.2:c.*214T= MANE Select	NP_004097.1:n.*214T=