Canonical Allele Identifier: CA342103880
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs1652644450

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152313898T>C , CM000663.2:g.152313898T>C GRCh38
NC_000001.10:g.152286374T>C , CM000663.1:g.152286374T>C GRCh37
NC_000001.9:g.150552998T>C NCBI36
NG_016190.1:g.16306A>G , LRG_1028:g.16306A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000368799.2:c.988A>G MANE Select ENSP00000357789.1:p.Arg330Gly
ENST00000368799.1:c.988A>G ENSP00000357789.1:p.Arg330Gly
NM_002016.1:c.988A>G , LRG_1028t1:c.988A>G NP_002007.1:p.Arg330Gly
NR_103778.1:n.440T>C
XM_011509329.1:c.988A>G XP_011507631.1:p.Arg330Gly
NM_002016.2:c.988A>G MANE Select NP_002007.1:p.Arg330Gly