Canonical Allele Identifier: CA1107247
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs758594800

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152312592T>A , CM000663.2:g.152312592T>A GRCh38
NC_000001.10:g.152285068T>A , CM000663.1:g.152285068T>A GRCh37
NC_000001.9:g.150551692T>A NCBI36
NG_016190.1:g.17612A>T , LRG_1028:g.17612A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.2294A>T MANE Select ENSP00000357789.1:p.His765Leu
ENST00000368799.1:c.2294A>T ENSP00000357789.1:p.His765Leu
NM_002016.1:c.2294A>T , LRG_1028t1:c.2294A>T NP_002007.1:p.His765Leu
XM_011509329.1:c.2294A>T XP_011507631.1:p.His765Leu
NM_002016.2:c.2294A>T MANE Select NP_002007.1:p.His765Leu