Canonical Allele Identifier: CA31357249
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs904309750
MyVariant Identifiers: chr1:g.159258330C>T (hg19) chr1:g.159288540C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159288540C>T , CM000663.2:g.159288540C>T GRCh38
NC_000001.10:g.159258330C>T , CM000663.1:g.159258330C>T GRCh37
NC_000001.9:g.157524954C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_002001.3:c.-97-1176C>T NP_001992.1:n.-97-1176C>T
NM_002001.4:c.-97-1176C>T NP_001992.1:n.-97-1176C>T
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