Canonical Allele Identifier: CA30602941
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs918420067

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152305057G>A , CM000663.2:g.152305057G>A GRCh38
NC_000001.10:g.152277533G>A , CM000663.1:g.152277533G>A GRCh37
NC_000001.9:g.150544157G>A NCBI36
NG_016190.1:g.25147C>T , LRG_1028:g.25147C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.9829C>T MANE Select ENSP00000357789.1:p.Arg3277Cys
ENST00000368799.1:c.9829C>T ENSP00000357789.1:p.Arg3277Cys
NM_002016.1:c.9829C>T , LRG_1028t1:c.9829C>T NP_002007.1:p.Arg3277Cys
XM_011509329.1:c.9108+721C>T XP_011507631.1:n.9108+721C>T
NM_002016.2:c.9829C>T MANE Select NP_002007.1:p.Arg3277Cys