Canonical Allele Identifier: CA1201822701
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs1652072385

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159288518C>T , CM000663.2:g.159288518C>T GRCh38
NC_000001.10:g.159258308C>T , CM000663.1:g.159258308C>T GRCh37
NC_000001.9:g.157524932C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_002001.3:c.-97-1198C>T NP_001992.1:n.-97-1198C>T
NM_002001.4:c.-97-1198C>T NP_001992.1:n.-97-1198C>T