Canonical Allele Identifier: CA342069418
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs771594459

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304385G>A , CM000663.2:g.152304385G>A GRCh38
NC_000001.10:g.152276861G>A , CM000663.1:g.152276861G>A GRCh37
NC_000001.9:g.150543485G>A NCBI36
NG_016190.1:g.25819C>T , LRG_1028:g.25819C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.10501C>T MANE Select ENSP00000357789.1:p.His3501Tyr
ENST00000368799.1:c.10501C>T ENSP00000357789.1:p.His3501Tyr
NM_002016.1:c.10501C>T , LRG_1028t1:c.10501C>T NP_002007.1:p.His3501Tyr
XM_011509329.1:c.9109-552C>T XP_011507631.1:n.9109-552C>T
NM_002016.2:c.10501C>T MANE Select NP_002007.1:p.His3501Tyr