Canonical Allele Identifier: CA1201830741
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs1652449310

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159302242G>A , CM000663.2:g.159302242G>A GRCh38
NC_000001.10:g.159272032G>A , CM000663.1:g.159272032G>A GRCh37
NC_000001.9:g.157538656G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368115.5:c.-59-64G>A ENSP00000357097.1:n.-59-64G>A
NM_002001.3:c.-59-64G>A NP_001992.1:n.-59-64G>A
NM_002001.4:c.-59-64G>A NP_001992.1:n.-59-64G>A