Canonical Allele Identifier: CA1201822785
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs1305410012

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159288631C>A , CM000663.2:g.159288631C>A GRCh38
NC_000001.10:g.159258421C>A , CM000663.1:g.159258421C>A GRCh37
NC_000001.9:g.157525045C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_002001.3:c.-97-1085C>A NP_001992.1:n.-97-1085C>A
NM_002001.4:c.-97-1085C>A NP_001992.1:n.-97-1085C>A