Canonical Allele Identifier: CA340249349
Gene: FOXE3 HGNC NCBI
LINC01389 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.47882245C>A (hg19) chr1:g.47416573C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.47416573C>A , CM000663.2:g.47416573C>A GRCh38
NC_000001.10:g.47882245C>A , CM000663.1:g.47882245C>A GRCh37
NC_000001.9:g.47654832C>A NCBI36
NG_016192.1:g.5502C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000335071.4:c.258C>A (FOXE3) MANE Select ENSP00000334472.2:p.His86Gln
ENST00000335071.3:c.258C>A (FOXE3) ENSP00000334472.2:p.His86Gln
NM_012186.2:c.258C>A (FOXE3) NP_036318.1:p.His86Gln
NR_126355.1:n.29-6672G>T (LINC01389)
NM_012186.3:c.258C>A (FOXE3) MANE Select NP_036318.1:p.His86Gln
Search 100 bp 5'
Search 100 bp 3'