Canonical Allele Identifier: CA1105335
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs146352383
ExAC: 1:152281106 G / A
gnomAD v2: 1-152281106-G-A
gnomAD v3: 1-152308630-G-A
gnomAD v4: 1-152308630-G-A
COSMIC: COSM218327
MyVariant Identifiers: chr1:g.152281106G>A (hg19) chr1:g.152308630G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152308630G>A , CM000663.2:g.152308630G>A GRCh38
NC_000001.10:g.152281106G>A , CM000663.1:g.152281106G>A GRCh37
NC_000001.9:g.150547730G>A NCBI36
NG_016190.1:g.21574C>T , LRG_1028:g.21574C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.6256C>T MANE Select ENSP00000357789.1:p.Arg2086Cys
ENST00000368799.1:c.6256C>T ENSP00000357789.1:p.Arg2086Cys
NM_002016.1:c.6256C>T , LRG_1028t1:c.6256C>T NP_002007.1:p.Arg2086Cys
XM_011509329.1:c.6256C>T XP_011507631.1:p.Arg2086Cys
NM_002016.2:c.6256C>T MANE Select NP_002007.1:p.Arg2086Cys
Search 100 bp 5'
Search 100 bp 3'