Canonical Allele Identifier: CA1008275925
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs1652446247

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159302107_159302108del , CM000663.2:g.159302107_159302108del GRCh38
NC_000001.10:g.159271897_159271898del , CM000663.1:g.159271897_159271898del GRCh37
NC_000001.9:g.157538521_157538522del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368115.5:c.-59-199_-59-198del ENSP00000357097.1:n.-59-199_-59-198del
NM_002001.3:c.-59-199_-59-198del NP_001992.1:n.-59-199_-59-198del
NM_002001.4:c.-59-199_-59-198del NP_001992.1:n.-59-199_-59-198del