Canonical Allele Identifier: CA645917622
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs1652445940
gnomAD v3: 1-159302091-C-T
gnomAD v4: 1-159302091-C-T
COSMIC: COSN16683863
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159302091C>T , CM000663.2:g.159302091C>T GRCh38
NC_000001.10:g.159271881C>T , CM000663.1:g.159271881C>T GRCh37
NC_000001.9:g.157538505C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368115.5:c.-59-215C>T ENSP00000357097.1:n.-59-215C>T
NM_002001.3:c.-59-215C>T NP_001992.1:n.-59-215C>T
NM_002001.4:c.-59-215C>T NP_001992.1:n.-59-215C>T
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