Canonical Allele Identifier: CA497013753
Gene: FOXF1 HGNC NCBI

Linked Data

dbSNP Id: rs1323320290

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.86510854C>G , CM000678.2:g.86510854C>G GRCh38
NC_000016.9:g.86544460C>G , CM000678.1:g.86544460C>G GRCh37
NC_000016.8:g.85101961C>G NCBI36
NG_016273.1:g.5328C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262426.6:c.285C>G MANE Select ENSP00000262426.4:p.Ser95=
ENST00000262426.5:c.285C>G ENSP00000262426.4:p.Ser95=
NM_001451.2:c.285C>G NP_001442.2:p.Ser95=
NM_001451.3:c.285C>G MANE Select NP_001442.2:p.Ser95=