Canonical Allele Identifier: CA420932268
Gene: FLG HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.152286486A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152314010A>G , CM000663.2:g.152314010A>G GRCh38
NC_000001.10:g.152286486A>G , CM000663.1:g.152286486A>G GRCh37
NC_000001.9:g.150553110A>G NCBI36
NG_016190.1:g.16194T>C , LRG_1028:g.16194T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000368799.2:c.876T>C MANE Select ENSP00000357789.1:p.Arg292=
ENST00000368799.1:c.876T>C ENSP00000357789.1:p.Arg292=
NM_002016.1:c.876T>C , LRG_1028t1:c.876T>C NP_002007.1:p.Arg292=
NR_103778.1:n.552A>G
XM_011509329.1:c.876T>C XP_011507631.1:p.Arg292=
NM_002016.2:c.876T>C MANE Select NP_002007.1:p.Arg292=
Search 100 bp 5'
Search 100 bp 3'