Canonical Allele Identifier: CA342074520
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs12732920

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152310476A>T , CM000663.2:g.152310476A>T GRCh38
NC_000001.10:g.152282952A>T , CM000663.1:g.152282952A>T GRCh37
NC_000001.9:g.150549576A>T NCBI36
NG_016190.1:g.19728T>A , LRG_1028:g.19728T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.4410T>A MANE Select ENSP00000357789.1:p.His1470Gln
ENST00000368799.1:c.4410T>A ENSP00000357789.1:p.His1470Gln
NM_002016.1:c.4410T>A , LRG_1028t1:c.4410T>A NP_002007.1:p.His1470Gln
XM_011509329.1:c.4410T>A XP_011507631.1:p.His1470Gln
NM_002016.2:c.4410T>A MANE Select NP_002007.1:p.His1470Gln