Canonical Allele Identifier: CA1201822861
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs1652078041

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159288725C>G , CM000663.2:g.159288725C>G GRCh38
NC_000001.10:g.159258515C>G , CM000663.1:g.159258515C>G GRCh37
NC_000001.9:g.157525139C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_002001.3:c.-97-991C>G NP_001992.1:n.-97-991C>G
NM_002001.4:c.-97-991C>G NP_001992.1:n.-97-991C>G