Canonical Allele Identifier: CA1201830663
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs1652445231

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159302076A>C , CM000663.2:g.159302076A>C GRCh38
NC_000001.10:g.159271866A>C , CM000663.1:g.159271866A>C GRCh37
NC_000001.9:g.157538490A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000368115.5:c.-59-230A>C ENSP00000357097.1:n.-59-230A>C
NM_002001.3:c.-59-230A>C NP_001992.1:n.-59-230A>C
NM_002001.4:c.-59-230A>C NP_001992.1:n.-59-230A>C