Canonical Allele Identifier: CA1103442
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs751970988

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304623G>C , CM000663.2:g.152304623G>C GRCh38
NC_000001.10:g.152277099G>C , CM000663.1:g.152277099G>C GRCh37
NC_000001.9:g.150543723G>C NCBI36
NG_016190.1:g.25581C>G , LRG_1028:g.25581C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.10263C>G MANE Select ENSP00000357789.1:p.Ser3421Arg
ENST00000368799.1:c.10263C>G ENSP00000357789.1:p.Ser3421Arg
NM_002016.1:c.10263C>G , LRG_1028t1:c.10263C>G NP_002007.1:p.Ser3421Arg
XM_011509329.1:c.9109-790C>G XP_011507631.1:n.9109-790C>G
NM_002016.2:c.10263C>G MANE Select NP_002007.1:p.Ser3421Arg