Canonical Allele Identifier: CA526865503
Gene: FCER1G HGNC NCBI

Linked Data

dbSNP Id: rs1372646016
gnomAD v2: 1-161188951-G-C
gnomAD v3: 1-161219161-G-C
gnomAD v4: 1-161219161-G-C
MyVariant Identifiers: chr1:g.161188951G>C (hg19) chr1:g.161219161G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161219161G>C , CM000663.2:g.161219161G>C GRCh38
NC_000001.10:g.161188951G>C , CM000663.1:g.161188951G>C GRCh37
NC_000001.9:g.159455575G>C NCBI36
NG_029043.1:g.8865G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000289902.2:c.*218G>C MANE Select ENSP00000289902.1:n.*218G>C
ENST00000289902.1:c.*218G>C ENSP00000289902.1:n.*218G>C
ENST00000367992.7:c.198+438G>C ENSP00000356971.3:n.198+438G>C
ENST00000490414.1:n.475G>C
NM_004106.1:c.*218G>C NP_004097.1:n.*218G>C
NM_004106.2:c.*218G>C MANE Select NP_004097.1:n.*218G>C
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