Canonical Allele Identifier: CA1008275892
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs1652442203
gnomAD v3: 1-159301963-G-A
gnomAD v4: 1-159301963-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159301963G>A , CM000663.2:g.159301963G>A GRCh38
NC_000001.10:g.159271753G>A , CM000663.1:g.159271753G>A GRCh37
NC_000001.9:g.157538377G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368115.5:c.-59-343G>A ENSP00000357097.1:n.-59-343G>A
NM_002001.3:c.-59-343G>A NP_001992.1:n.-59-343G>A
NM_002001.4:c.-59-343G>A NP_001992.1:n.-59-343G>A
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