Canonical Allele Identifier: CA1201822929
Gene: FCER1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159288827G= , CM000663.2:g.159288827G= GRCh38
NC_000001.10:g.159258617G= , CM000663.1:g.159258617G= GRCh37
NC_000001.9:g.157525241G= NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_002001.3:c.-97-889G= NP_001992.1:n.-97-889G=
NM_002001.4:c.-97-889G= NP_001992.1:n.-97-889G=