Canonical Allele Identifier: CA342073703
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs1353933532
gnomAD v2: 1-152277329-C-T
gnomAD v3: 1-152304853-C-T
gnomAD v4: 1-152304853-C-T
COSMIC: COSM3473967
MyVariant Identifiers: chr1:g.152277329C>T (hg19) chr1:g.152304853C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304853C>T , CM000663.2:g.152304853C>T GRCh38
NC_000001.10:g.152277329C>T , CM000663.1:g.152277329C>T GRCh37
NC_000001.9:g.150543953C>T NCBI36
NG_016190.1:g.25351G>A , LRG_1028:g.25351G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.10033G>A MANE Select ENSP00000357789.1:p.Gly3345Arg
ENST00000368799.1:c.10033G>A ENSP00000357789.1:p.Gly3345Arg
NM_002016.1:c.10033G>A , LRG_1028t1:c.10033G>A NP_002007.1:p.Gly3345Arg
XM_011509329.1:c.9108+925G>A XP_011507631.1:n.9108+925G>A
NM_002016.2:c.10033G>A MANE Select NP_002007.1:p.Gly3345Arg
Search 100 bp 5'
Search 100 bp 3'