Canonical Allele Identifier: CA890191852
Gene: FCER1G HGNC NCBI

Linked Data

dbSNP Id: rs1429933244
gnomAD v4: 1-161219053-T-C
MyVariant Identifiers: chr1:g.161188843T>C (hg19) chr1:g.161219053T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161219053T>C , CM000663.2:g.161219053T>C GRCh38
NC_000001.10:g.161188843T>C , CM000663.1:g.161188843T>C GRCh37
NC_000001.9:g.159455467T>C NCBI36
NG_029043.1:g.8757T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000289902.2:c.*110T>C MANE Select ENSP00000289902.1:n.*110T>C
ENST00000289902.1:c.*110T>C ENSP00000289902.1:n.*110T>C
ENST00000367992.7:c.198+330T>C ENSP00000356971.3:n.198+330T>C
ENST00000490414.1:n.367T>C
NM_004106.1:c.*110T>C NP_004097.1:n.*110T>C
NM_004106.2:c.*110T>C MANE Select NP_004097.1:n.*110T>C
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