Canonical Allele Identifier: CA31632455
Gene: FCER1G HGNC NCBI

Linked Data

dbSNP Id: rs1000534798
gnomAD v3: 1-161219152-C-T
gnomAD v4: 1-161219152-C-T
MyVariant Identifiers: chr1:g.161188942C>T (hg19) chr1:g.161219152C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161219152C>T , CM000663.2:g.161219152C>T GRCh38
NC_000001.10:g.161188942C>T , CM000663.1:g.161188942C>T GRCh37
NC_000001.9:g.159455566C>T NCBI36
NG_029043.1:g.8856C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000289902.2:c.*209C>T MANE Select ENSP00000289902.1:n.*209C>T
ENST00000289902.1:c.*209C>T ENSP00000289902.1:n.*209C>T
ENST00000367992.7:c.198+429C>T ENSP00000356971.3:n.198+429C>T
ENST00000490414.1:n.466C>T
NM_004106.1:c.*209C>T NP_004097.1:n.*209C>T
NM_004106.2:c.*209C>T MANE Select NP_004097.1:n.*209C>T
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