Canonical Allele Identifier: CA342089649
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs1652514999

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152312447G>C , CM000663.2:g.152312447G>C GRCh38
NC_000001.10:g.152284923G>C , CM000663.1:g.152284923G>C GRCh37
NC_000001.9:g.150551547G>C NCBI36
NG_016190.1:g.17757C>G , LRG_1028:g.17757C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.2439C>G MANE Select ENSP00000357789.1:p.Ser813Arg
ENST00000368799.1:c.2439C>G ENSP00000357789.1:p.Ser813Arg
NM_002016.1:c.2439C>G , LRG_1028t1:c.2439C>G NP_002007.1:p.Ser813Arg
XM_011509329.1:c.2439C>G XP_011507631.1:p.Ser813Arg
NM_002016.2:c.2439C>G MANE Select NP_002007.1:p.Ser813Arg