Canonical Allele Identifier: CA1201830755
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs1652450629

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159302277A>T , CM000663.2:g.159302277A>T GRCh38
NC_000001.10:g.159272067A>T , CM000663.1:g.159272067A>T GRCh37
NC_000001.9:g.157538691A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368115.5:c.-59-29A>T ENSP00000357097.1:n.-59-29A>T
NM_002001.3:c.-59-29A>T NP_001992.1:n.-59-29A>T
NM_002001.4:c.-59-29A>T NP_001992.1:n.-59-29A>T