Canonical Allele Identifier: CA1107108
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs376251735

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152312327C>G , CM000663.2:g.152312327C>G GRCh38
NC_000001.10:g.152284803C>G , CM000663.1:g.152284803C>G GRCh37
NC_000001.9:g.150551427C>G NCBI36
NG_016190.1:g.17877G>C , LRG_1028:g.17877G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.2559G>C MANE Select ENSP00000357789.1:p.Gln853His
ENST00000368799.1:c.2559G>C ENSP00000357789.1:p.Gln853His
NM_002016.1:c.2559G>C , LRG_1028t1:c.2559G>C NP_002007.1:p.Gln853His
XM_011509329.1:c.2559G>C XP_011507631.1:p.Gln853His
NM_002016.2:c.2559G>C MANE Select NP_002007.1:p.Gln853His