Canonical Allele Identifier: CA1201822792
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs1652075904

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159288642T>G , CM000663.2:g.159288642T>G GRCh38
NC_000001.10:g.159258432T>G , CM000663.1:g.159258432T>G GRCh37
NC_000001.9:g.157525056T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_002001.3:c.-97-1074T>G NP_001992.1:n.-97-1074T>G
NM_002001.4:c.-97-1074T>G NP_001992.1:n.-97-1074T>G