Canonical Allele Identifier: CA1106683
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2639297
ClinVar RCV Id: RCV003408991
dbSNP Id: rs376703034
ExAC: 1:152283926 G / T
gnomAD v2: 1-152283926-G-T
gnomAD v3: 1-152311450-G-T
gnomAD v4: 1-152311450-G-T
MyVariant Identifiers: chr1:g.152283926G>T (hg19) chr1:g.152311450G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152311450G>T , CM000663.2:g.152311450G>T GRCh38
NC_000001.10:g.152283926G>T , CM000663.1:g.152283926G>T GRCh37
NC_000001.9:g.150550550G>T NCBI36
NG_016190.1:g.18754C>A , LRG_1028:g.18754C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.3436C>A MANE Select ENSP00000357789.1:p.His1146Asn
ENST00000368799.1:c.3436C>A ENSP00000357789.1:p.His1146Asn
NM_002016.1:c.3436C>A , LRG_1028t1:c.3436C>A NP_002007.1:p.His1146Asn
XM_011509329.1:c.3436C>A XP_011507631.1:p.His1146Asn
NM_002016.2:c.3436C>A MANE Select NP_002007.1:p.His1146Asn
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