Canonical Allele Identifier: CA31364558
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs1000886233
gnomAD v4: 1-159302307-C-G
MyVariant Identifiers: chr1:g.159272097C>G (hg19) chr1:g.159302307C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159302307C>G , CM000663.2:g.159302307C>G GRCh38
NC_000001.10:g.159272097C>G , CM000663.1:g.159272097C>G GRCh37
NC_000001.9:g.157538721C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368115.5:c.-58C>G ENSP00000357097.1:n.-58C>G
NM_002001.3:c.-58C>G NP_001992.1:n.-58C>G
NM_002001.4:c.-58C>G NP_001992.1:n.-58C>G
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