Canonical Allele Identifier: CA2648764989
Gene: FCER1G HGNC NCBI

Linked Data

gnomAD v4: 1-161219131-CG-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161219133del , CM000663.2:g.161219133del GRCh38
NC_000001.10:g.161188923del , CM000663.1:g.161188923del GRCh37
NC_000001.9:g.159455547del NCBI36
NG_029043.1:g.8837del

Transcript Alleles

HGVS Amino-acid Change
ENST00000289902.2:c.*190del MANE Select ENSP00000289902.1:n.*190del
ENST00000289902.1:c.*190del ENSP00000289902.1:n.*190del
ENST00000367992.7:c.198+410del ENSP00000356971.3:n.198+410del
ENST00000490414.1:n.447del
NM_004106.1:c.*190del NP_004097.1:n.*190del
NM_004106.2:c.*190del MANE Select NP_004097.1:n.*190del
Search 100 bp 5'
Search 100 bp 3'