Canonical Allele Identifier: CA1201830609
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs1571080287

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159301917T>A , CM000663.2:g.159301917T>A GRCh38
NC_000001.10:g.159271707T>A , CM000663.1:g.159271707T>A GRCh37
NC_000001.9:g.157538331T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368115.5:c.-59-389T>A ENSP00000357097.1:n.-59-389T>A
NM_002001.3:c.-59-389T>A NP_001992.1:n.-59-389T>A
NM_002001.4:c.-59-389T>A NP_001992.1:n.-59-389T>A