Canonical Allele Identifier: CA466359986
Gene: FOXE1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.100616280G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97853998G>C , CM000671.2:g.97853998G>C GRCh38
NC_000009.11:g.100616280G>C , CM000671.1:g.100616280G>C GRCh37
NC_000009.10:g.99656101G>C NCBI36
NG_011979.1:g.5744G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375123.5:c.84G>C MANE Select ENSP00000364265.3:p.Gly28=
ENST00000375123.4:c.84G>C ENSP00000364265.3:p.Gly28=
NM_004473.3:c.84G>C NP_004464.2:p.Gly28=
NM_004473.4:c.84G>C MANE Select NP_004464.2:p.Gly28=
Search 100 bp 5'
Search 100 bp 3'