Canonical Allele Identifier: CA1202650821
Gene: FCER1G HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161219049C= , CM000663.2:g.161219049C= GRCh38
NC_000001.10:g.161188839C= , CM000663.1:g.161188839C= GRCh37
NC_000001.9:g.159455463C= NCBI36
NG_029043.1:g.8753C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000289902.2:c.*106C= MANE Select ENSP00000289902.1:n.*106C=
ENST00000289902.1:c.*106C= ENSP00000289902.1:n.*106C=
ENST00000367992.7:c.198+326C= ENSP00000356971.3:n.198+326C=
ENST00000490414.1:n.363C=
NM_004106.1:c.*106C= NP_004097.1:n.*106C=
NM_004106.2:c.*106C= MANE Select NP_004097.1:n.*106C=
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