Canonical Allele Identifier: CA31632395
Gene: FCER1G HGNC NCBI

Linked Data

dbSNP Id: rs896569455
gnomAD v4: 1-161219048-C-A
MyVariant Identifiers: chr1:g.161188838C>A (hg19) chr1:g.161219048C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161219048C>A , CM000663.2:g.161219048C>A GRCh38
NC_000001.10:g.161188838C>A , CM000663.1:g.161188838C>A GRCh37
NC_000001.9:g.159455462C>A NCBI36
NG_029043.1:g.8752C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000289902.2:c.*105C>A MANE Select ENSP00000289902.1:n.*105C>A
ENST00000289902.1:c.*105C>A ENSP00000289902.1:n.*105C>A
ENST00000367992.7:c.198+325C>A ENSP00000356971.3:n.198+325C>A
ENST00000490414.1:n.362C>A
NM_004106.1:c.*105C>A NP_004097.1:n.*105C>A
NM_004106.2:c.*105C>A MANE Select NP_004097.1:n.*105C>A
Search 100 bp 5'
Search 100 bp 3'