Canonical Allele Identifier: CA30568281
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs772522029

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152313888G>T , CM000663.2:g.152313888G>T GRCh38
NC_000001.10:g.152286364G>T , CM000663.1:g.152286364G>T GRCh37
NC_000001.9:g.150552988G>T NCBI36
NG_016190.1:g.16316C>A , LRG_1028:g.16316C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000368799.2:c.998C>A MANE Select ENSP00000357789.1:p.Ser333Tyr
ENST00000368799.1:c.998C>A ENSP00000357789.1:p.Ser333Tyr
NM_002016.1:c.998C>A , LRG_1028t1:c.998C>A NP_002007.1:p.Ser333Tyr
NR_103778.1:n.430G>T
XM_011509329.1:c.998C>A XP_011507631.1:p.Ser333Tyr
NM_002016.2:c.998C>A MANE Select NP_002007.1:p.Ser333Tyr