Canonical Allele Identifier: CA890016194
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs1327676359
gnomAD v3: 1-159301911-A-T
gnomAD v4: 1-159301911-A-T
MyVariant Identifiers: chr1:g.159271701A>T (hg19) chr1:g.159301911A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159301911A>T , CM000663.2:g.159301911A>T GRCh38
NC_000001.10:g.159271701A>T , CM000663.1:g.159271701A>T GRCh37
NC_000001.9:g.157538325A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000368115.5:c.-59-395A>T ENSP00000357097.1:n.-59-395A>T
NM_002001.3:c.-59-395A>T NP_001992.1:n.-59-395A>T
NM_002001.4:c.-59-395A>T NP_001992.1:n.-59-395A>T
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