Canonical Allele Identifier: CA1105431
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2292483
ClinVar RCV Id: RCV002832497
dbSNP Id: rs770336889
ExAC: 1:152281295 C / A
gnomAD v2: 1-152281295-C-A
gnomAD v3: 1-152308819-C-A
gnomAD v4: 1-152308819-C-A
MyVariant Identifiers: chr1:g.152281295C>A (hg19) chr1:g.152308819C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152308819C>A , CM000663.2:g.152308819C>A GRCh38
NC_000001.10:g.152281295C>A , CM000663.1:g.152281295C>A GRCh37
NC_000001.9:g.150547919C>A NCBI36
NG_016190.1:g.21385G>T , LRG_1028:g.21385G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.6067G>T MANE Select ENSP00000357789.1:p.Gly2023Trp
ENST00000368799.1:c.6067G>T ENSP00000357789.1:p.Gly2023Trp
NM_002016.1:c.6067G>T , LRG_1028t1:c.6067G>T NP_002007.1:p.Gly2023Trp
XM_011509329.1:c.6067G>T XP_011507631.1:p.Gly2023Trp
NM_002016.2:c.6067G>T MANE Select NP_002007.1:p.Gly2023Trp
Search 100 bp 5'
Search 100 bp 3'