Canonical Allele Identifier: CA10960701
Gene: FCER1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159295272T>C , CM000663.2:g.159295272T>C GRCh38
NC_000001.10:g.159265062T>C , CM000663.1:g.159265062T>C GRCh37
NC_000001.9:g.157531686T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368115.5:c.-60+5519T>C ENSP00000357097.1:n.-60+5519T>C
NM_002001.3:c.-60+5519T>C NP_001992.1:n.-60+5519T>C
NM_002001.4:c.-60+5519T>C NP_001992.1:n.-60+5519T>C