Canonical Allele Identifier: CA869020413
Gene: FOXE1 HGNC NCBI

Linked Data

dbSNP Id: rs1162406129
gnomAD v3: 9-97853896-G-A
gnomAD v4: 9-97853896-G-A
MyVariant Identifiers: chr9:g.100616178G>A (hg19) chr9:g.97853896G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97853896G>A , CM000671.2:g.97853896G>A GRCh38
NC_000009.11:g.100616178G>A , CM000671.1:g.100616178G>A GRCh37
NC_000009.10:g.99655999G>A NCBI36
NG_011979.1:g.5642G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375123.5:c.-19G>A MANE Select ENSP00000364265.3:n.-19G>A
ENST00000375123.4:c.-19G>A ENSP00000364265.3:n.-19G>A
NM_004473.3:c.-19G>A NP_004464.2:n.-19G>A
NM_004473.4:c.-19G>A MANE Select NP_004464.2:n.-19G>A
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