Canonical Allele Identifier: CA31364435
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs543384086
MyVariant Identifiers: chr1:g.159271906T>G (hg19) chr1:g.159302116T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159302116T>G , CM000663.2:g.159302116T>G GRCh38
NC_000001.10:g.159271906T>G , CM000663.1:g.159271906T>G GRCh37
NC_000001.9:g.157538530T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368115.5:c.-59-190T>G ENSP00000357097.1:n.-59-190T>G
NM_002001.3:c.-59-190T>G NP_001992.1:n.-59-190T>G
NM_002001.4:c.-59-190T>G NP_001992.1:n.-59-190T>G
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