Canonical Allele Identifier: CA31364431
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs145038112

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159302106_159302111del , CM000663.2:g.159302106_159302111del GRCh38
NC_000001.10:g.159271896_159271901del , CM000663.1:g.159271896_159271901del GRCh37
NC_000001.9:g.157538520_157538525del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368115.5:c.-59-200_-59-195del ENSP00000357097.1:n.-59-200_-59-195del
NM_002001.3:c.-59-200_-59-195del NP_001992.1:n.-59-200_-59-195del
NM_002001.4:c.-59-200_-59-195del NP_001992.1:n.-59-200_-59-195del