Canonical Allele Identifier: CA2648764920
Gene: FCER1G HGNC NCBI

Linked Data

gnomAD v4: 1-161219080-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161219080A>C , CM000663.2:g.161219080A>C GRCh38
NC_000001.10:g.161188870A>C , CM000663.1:g.161188870A>C GRCh37
NC_000001.9:g.159455494A>C NCBI36
NG_029043.1:g.8784A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000289902.2:c.*137A>C MANE Select ENSP00000289902.1:n.*137A>C
ENST00000289902.1:c.*137A>C ENSP00000289902.1:n.*137A>C
ENST00000367992.7:c.198+357A>C ENSP00000356971.3:n.198+357A>C
ENST00000490414.1:n.394A>C
NM_004106.1:c.*137A>C NP_004097.1:n.*137A>C
NM_004106.2:c.*137A>C MANE Select NP_004097.1:n.*137A>C
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