Canonical Allele Identifier: CA890016180
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs563134356
gnomAD v3: 1-159301867-C-A
gnomAD v4: 1-159301867-C-A
MyVariant Identifiers: chr1:g.159271657C>A (hg19) chr1:g.159301867C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159301867C>A , CM000663.2:g.159301867C>A GRCh38
NC_000001.10:g.159271657C>A , CM000663.1:g.159271657C>A GRCh37
NC_000001.9:g.157538281C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000368115.5:c.-59-439C>A ENSP00000357097.1:n.-59-439C>A
NM_002001.3:c.-59-439C>A NP_001992.1:n.-59-439C>A
NM_002001.4:c.-59-439C>A NP_001992.1:n.-59-439C>A
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