Canonical Allele Identifier: CA342057745
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2639280
ClinVar RCV Id: RCV003408974
MyVariant Identifiers: chr1:g.152281258C>A (hg19) chr1:g.152308782C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152308782C>A , CM000663.2:g.152308782C>A GRCh38
NC_000001.10:g.152281258C>A , CM000663.1:g.152281258C>A GRCh37
NC_000001.9:g.150547882C>A NCBI36
NG_016190.1:g.21422G>T , LRG_1028:g.21422G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.6104G>T MANE Select ENSP00000357789.1:p.Gly2035Val
ENST00000368799.1:c.6104G>T ENSP00000357789.1:p.Gly2035Val
NM_002016.1:c.6104G>T , LRG_1028t1:c.6104G>T NP_002007.1:p.Gly2035Val
XM_011509329.1:c.6104G>T XP_011507631.1:p.Gly2035Val
NM_002016.2:c.6104G>T MANE Select NP_002007.1:p.Gly2035Val
Search 100 bp 5'
Search 100 bp 3'