Canonical Allele Identifier: CA1201822796
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs1571073626

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159288644A>C , CM000663.2:g.159288644A>C GRCh38
NC_000001.10:g.159258434A>C , CM000663.1:g.159258434A>C GRCh37
NC_000001.9:g.157525058A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_002001.3:c.-97-1072A>C NP_001992.1:n.-97-1072A>C
NM_002001.4:c.-97-1072A>C NP_001992.1:n.-97-1072A>C