Canonical Allele Identifier: CA890016249
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs1177067623

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159302067C>T , CM000663.2:g.159302067C>T GRCh38
NC_000001.10:g.159271857C>T , CM000663.1:g.159271857C>T GRCh37
NC_000001.9:g.157538481C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000368115.5:c.-59-239C>T ENSP00000357097.1:n.-59-239C>T
NM_002001.3:c.-59-239C>T NP_001992.1:n.-59-239C>T
NM_002001.4:c.-59-239C>T NP_001992.1:n.-59-239C>T