Canonical Allele Identifier: CA420930810
Gene: FLG HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.152284740G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152312264G>A , CM000663.2:g.152312264G>A GRCh38
NC_000001.10:g.152284740G>A , CM000663.1:g.152284740G>A GRCh37
NC_000001.9:g.150551364G>A NCBI36
NG_016190.1:g.17940C>T , LRG_1028:g.17940C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.2622C>T MANE Select ENSP00000357789.1:p.Thr874=
ENST00000368799.1:c.2622C>T ENSP00000357789.1:p.Thr874=
NM_002016.1:c.2622C>T , LRG_1028t1:c.2622C>T NP_002007.1:p.Thr874=
XM_011509329.1:c.2622C>T XP_011507631.1:p.Thr874=
NM_002016.2:c.2622C>T MANE Select NP_002007.1:p.Thr874=
Search 100 bp 5'
Search 100 bp 3'