Canonical Allele Identifier: CA1201822713
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs1652072661

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159288532T>C , CM000663.2:g.159288532T>C GRCh38
NC_000001.10:g.159258322T>C , CM000663.1:g.159258322T>C GRCh37
NC_000001.9:g.157524946T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_002001.3:c.-97-1184T>C NP_001992.1:n.-97-1184T>C
NM_002001.4:c.-97-1184T>C NP_001992.1:n.-97-1184T>C