Canonical Allele Identifier: CA1103364
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs769609196
ExAC: 1:152276962 G / T
gnomAD v2: 1-152276962-G-T
gnomAD v3: 1-152304486-G-T
gnomAD v4: 1-152304486-G-T
MyVariant Identifiers: chr1:g.152276962G>T (hg19) chr1:g.152304486G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304486G>T , CM000663.2:g.152304486G>T GRCh38
NC_000001.10:g.152276962G>T , CM000663.1:g.152276962G>T GRCh37
NC_000001.9:g.150543586G>T NCBI36
NG_016190.1:g.25718C>A , LRG_1028:g.25718C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.10400C>A MANE Select ENSP00000357789.1:p.Thr3467Asn
ENST00000368799.1:c.10400C>A ENSP00000357789.1:p.Thr3467Asn
NM_002016.1:c.10400C>A , LRG_1028t1:c.10400C>A NP_002007.1:p.Thr3467Asn
XM_011509329.1:c.9109-653C>A XP_011507631.1:n.9109-653C>A
NM_002016.2:c.10400C>A MANE Select NP_002007.1:p.Thr3467Asn
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