Canonical Allele Identifier: CA31364305
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs12086637

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159301950T>G , CM000663.2:g.159301950T>G GRCh38
NC_000001.10:g.159271740T>G , CM000663.1:g.159271740T>G GRCh37
NC_000001.9:g.157538364T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000368115.5:c.-59-356T>G ENSP00000357097.1:n.-59-356T>G
NM_002001.3:c.-59-356T>G NP_001992.1:n.-59-356T>G
NM_002001.4:c.-59-356T>G NP_001992.1:n.-59-356T>G