Canonical Allele Identifier: CA1201828813
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs7548864

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159297465G>T , CM000663.2:g.159297465G>T GRCh38
NC_000001.10:g.159267255G>T , CM000663.1:g.159267255G>T GRCh37
NC_000001.9:g.157533879G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000368115.5:c.-59-4841G>T ENSP00000357097.1:n.-59-4841G>T
NM_002001.3:c.-59-4841G>T NP_001992.1:n.-59-4841G>T
NM_002001.4:c.-59-4841G>T NP_001992.1:n.-59-4841G>T