Canonical Allele Identifier: CA197059301
Gene: FOXE1 HGNC NCBI

Linked Data

dbSNP Id: rs908320588
gnomAD v2: 9-100616284-G-A
gnomAD v3: 9-97854002-G-A
gnomAD v4: 9-97854002-G-A
MyVariant Identifiers: chr9:g.100616284G>A (hg19) chr9:g.97854002G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97854002G>A , CM000671.2:g.97854002G>A GRCh38
NC_000009.11:g.100616284G>A , CM000671.1:g.100616284G>A GRCh37
NC_000009.10:g.99656105G>A NCBI36
NG_011979.1:g.5748G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000375123.5:c.88G>A MANE Select ENSP00000364265.3:p.Gly30Arg
ENST00000375123.4:c.88G>A ENSP00000364265.3:p.Gly30Arg
NM_004473.3:c.88G>A NP_004464.2:p.Gly30Arg
NM_004473.4:c.88G>A MANE Select NP_004464.2:p.Gly30Arg
Search 100 bp 5'
Search 100 bp 3'