Canonical Allele Identifier: CA1201822781
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs1652075570

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159288629A>G , CM000663.2:g.159288629A>G GRCh38
NC_000001.10:g.159258419A>G , CM000663.1:g.159258419A>G GRCh37
NC_000001.9:g.157525043A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_002001.3:c.-97-1087A>G NP_001992.1:n.-97-1087A>G
NM_002001.4:c.-97-1087A>G NP_001992.1:n.-97-1087A>G