Canonical Allele Identifier: CA1201830649
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs2427827

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159302021T>G , CM000663.2:g.159302021T>G GRCh38
NC_000001.10:g.159271811T>G , CM000663.1:g.159271811T>G GRCh37
NC_000001.9:g.157538435T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000368115.5:c.-59-285T>G ENSP00000357097.1:n.-59-285T>G
NM_002001.3:c.-59-285T>G NP_001992.1:n.-59-285T>G
NM_002001.4:c.-59-285T>G NP_001992.1:n.-59-285T>G