Canonical Allele Identifier: CA2648765060
Gene: FCER1G HGNC NCBI

Linked Data

gnomAD v4: 1-161219162-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161219165del , CM000663.2:g.161219165del GRCh38
NC_000001.10:g.161188955del , CM000663.1:g.161188955del GRCh37
NC_000001.9:g.159455579del NCBI36
NG_029043.1:g.8869del

Transcript Alleles

HGVS Amino-acid Change
ENST00000289902.2:c.*222del MANE Select ENSP00000289902.1:n.*222del
ENST00000289902.1:c.*222del ENSP00000289902.1:n.*222del
ENST00000367992.7:c.198+442del ENSP00000356971.3:n.198+442del
ENST00000490414.1:n.479del
NM_004106.1:c.*222del NP_004097.1:n.*222del
NM_004106.2:c.*222del MANE Select NP_004097.1:n.*222del
Search 100 bp 5'
Search 100 bp 3'