Canonical Allele Identifier: CA2648765051
Gene: FCER1G HGNC NCBI

Linked Data

gnomAD v4: 1-161219160-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161219160T>G , CM000663.2:g.161219160T>G GRCh38
NC_000001.10:g.161188950T>G , CM000663.1:g.161188950T>G GRCh37
NC_000001.9:g.159455574T>G NCBI36
NG_029043.1:g.8864T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000289902.2:c.*217T>G MANE Select ENSP00000289902.1:n.*217T>G
ENST00000289902.1:c.*217T>G ENSP00000289902.1:n.*217T>G
ENST00000367992.7:c.198+437T>G ENSP00000356971.3:n.198+437T>G
ENST00000490414.1:n.474T>G
NM_004106.1:c.*217T>G NP_004097.1:n.*217T>G
NM_004106.2:c.*217T>G MANE Select NP_004097.1:n.*217T>G
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