Canonical Allele Identifier: CA1106443
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs769313265

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152310958C>T , CM000663.2:g.152310958C>T GRCh38
NC_000001.10:g.152283434C>T , CM000663.1:g.152283434C>T GRCh37
NC_000001.9:g.150550058C>T NCBI36
NG_016190.1:g.19246G>A , LRG_1028:g.19246G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000368799.2:c.3928G>A MANE Select ENSP00000357789.1:p.Gly1310Arg
ENST00000368799.1:c.3928G>A ENSP00000357789.1:p.Gly1310Arg
NM_002016.1:c.3928G>A , LRG_1028t1:c.3928G>A NP_002007.1:p.Gly1310Arg
XM_011509329.1:c.3928G>A XP_011507631.1:p.Gly1310Arg
NM_002016.2:c.3928G>A MANE Select NP_002007.1:p.Gly1310Arg