Canonical Allele Identifier: CA890016263
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs913299750
MyVariant Identifiers: chr1:g.159271905C>T (hg19) chr1:g.159302115C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159302115C>T , CM000663.2:g.159302115C>T GRCh38
NC_000001.10:g.159271905C>T , CM000663.1:g.159271905C>T GRCh37
NC_000001.9:g.157538529C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368115.5:c.-59-191C>T ENSP00000357097.1:n.-59-191C>T
NM_002001.3:c.-59-191C>T NP_001992.1:n.-59-191C>T
NM_002001.4:c.-59-191C>T NP_001992.1:n.-59-191C>T
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