Canonical Allele Identifier: CA890016197
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs1398200428
MyVariant Identifiers: chr1:g.159271708T>C (hg19) chr1:g.159301918T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159301918T>C , CM000663.2:g.159301918T>C GRCh38
NC_000001.10:g.159271708T>C , CM000663.1:g.159271708T>C GRCh37
NC_000001.9:g.157538332T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368115.5:c.-59-388T>C ENSP00000357097.1:n.-59-388T>C
NM_002001.3:c.-59-388T>C NP_001992.1:n.-59-388T>C
NM_002001.4:c.-59-388T>C NP_001992.1:n.-59-388T>C
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