Canonical Allele Identifier: CA1103389
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs760806964
ExAC: 1:152277005 A / T
gnomAD v2: 1-152277005-A-T
gnomAD v4: 1-152304529-A-T
MyVariant Identifiers: chr1:g.152277005A>T (hg19) chr1:g.152304529A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304529A>T , CM000663.2:g.152304529A>T GRCh38
NC_000001.10:g.152277005A>T , CM000663.1:g.152277005A>T GRCh37
NC_000001.9:g.150543629A>T NCBI36
NG_016190.1:g.25675T>A , LRG_1028:g.25675T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.10357T>A MANE Select ENSP00000357789.1:p.Ser3453Thr
ENST00000368799.1:c.10357T>A ENSP00000357789.1:p.Ser3453Thr
NM_002016.1:c.10357T>A , LRG_1028t1:c.10357T>A NP_002007.1:p.Ser3453Thr
XM_011509329.1:c.9109-696T>A XP_011507631.1:n.9109-696T>A
NM_002016.2:c.10357T>A MANE Select NP_002007.1:p.Ser3453Thr
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