Canonical Allele Identifier: CA890013265
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs922113591

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159288759A>T , CM000663.2:g.159288759A>T GRCh38
NC_000001.10:g.159258549A>T , CM000663.1:g.159258549A>T GRCh37
NC_000001.9:g.157525173A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_002001.3:c.-97-957A>T NP_001992.1:n.-97-957A>T
NM_002001.4:c.-97-957A>T NP_001992.1:n.-97-957A>T