Canonical Allele Identifier: CA1008399271
Gene: FCER1G HGNC NCBI

Linked Data

dbSNP Id: rs1666110580
gnomAD v3: 1-161219063-G-A
gnomAD v4: 1-161219063-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161219063G>A , CM000663.2:g.161219063G>A GRCh38
NC_000001.10:g.161188853G>A , CM000663.1:g.161188853G>A GRCh37
NC_000001.9:g.159455477G>A NCBI36
NG_029043.1:g.8767G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000289902.2:c.*120G>A MANE Select ENSP00000289902.1:n.*120G>A
ENST00000289902.1:c.*120G>A ENSP00000289902.1:n.*120G>A
ENST00000367992.7:c.198+340G>A ENSP00000356971.3:n.198+340G>A
ENST00000490414.1:n.377G>A
NM_004106.1:c.*120G>A NP_004097.1:n.*120G>A
NM_004106.2:c.*120G>A MANE Select NP_004097.1:n.*120G>A
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