Canonical Allele Identifier: CA15132443
Gene: FCER1A HGNC NCBI
dbSNP:
2427837
gnomAD v2:
1:159258545 G / A
gnomAD v3:
1:159288755 G / A
gnomAD v4:
chr1-159288755-G-A
Joint Max Group AF 0.27887127 (NFE)
Genomes Max Group AF 0.27887127 (NFE)
MyVariant.info:
GRCh38 chr1:g.159288755G>A
GRCh37 chr1:g.159258545G>A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159288755G>A , CM000663.2:g.159288755G>A GRCh38
NC_000001.10:g.159258545G>A , CM000663.1:g.159258545G>A GRCh37
NC_000001.9:g.157525169G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_002001.3:c.-97-961G>A NP_001992.1:n.-97-961G>A
NM_002001.4:c.-97-961G>A NP_001992.1:n.-97-961G>A
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