Canonical Allele Identifier: CA342057682
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs200002200

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152308777G>C , CM000663.2:g.152308777G>C GRCh38
NC_000001.10:g.152281253G>C , CM000663.1:g.152281253G>C GRCh37
NC_000001.9:g.150547877G>C NCBI36
NG_016190.1:g.21427C>G , LRG_1028:g.21427C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.6109C>G MANE Select ENSP00000357789.1:p.Arg2037Gly
ENST00000368799.1:c.6109C>G ENSP00000357789.1:p.Arg2037Gly
NM_002016.1:c.6109C>G , LRG_1028t1:c.6109C>G NP_002007.1:p.Arg2037Gly
XM_011509329.1:c.6109C>G XP_011507631.1:p.Arg2037Gly
NM_002016.2:c.6109C>G MANE Select NP_002007.1:p.Arg2037Gly