Canonical Allele Identifier: CA374347024
Gene: FOXE1 HGNC NCBI

Linked Data

dbSNP Id: rs1830625790
MyVariant Identifiers: chr9:g.100616279G>T (hg19) chr9:g.97853997G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97853997G>T , CM000671.2:g.97853997G>T GRCh38
NC_000009.11:g.100616279G>T , CM000671.1:g.100616279G>T GRCh37
NC_000009.10:g.99656100G>T NCBI36
NG_011979.1:g.5743G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000375123.5:c.83G>T MANE Select ENSP00000364265.3:p.Gly28Val
ENST00000375123.4:c.83G>T ENSP00000364265.3:p.Gly28Val
NM_004473.3:c.83G>T NP_004464.2:p.Gly28Val
NM_004473.4:c.83G>T MANE Select NP_004464.2:p.Gly28Val
Search 100 bp 5'
Search 100 bp 3'