Canonical Allele Identifier: CA1202650838
Gene: FCER1G HGNC NCBI

Linked Data

dbSNP Id: rs755927809
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161219115G>A , CM000663.2:g.161219115G>A GRCh38
NC_000001.10:g.161188905G>A , CM000663.1:g.161188905G>A GRCh37
NC_000001.9:g.159455529G>A NCBI36
NG_029043.1:g.8819G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000289902.2:c.*172G>A MANE Select ENSP00000289902.1:n.*172G>A
ENST00000289902.1:c.*172G>A ENSP00000289902.1:n.*172G>A
ENST00000367992.7:c.198+392G>A ENSP00000356971.3:n.198+392G>A
ENST00000490414.1:n.429G>A
NM_004106.1:c.*172G>A NP_004097.1:n.*172G>A
NM_004106.2:c.*172G>A MANE Select NP_004097.1:n.*172G>A
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