Canonical Allele Identifier: CA420926707
Gene: FLG HGNC NCBI

Linked Data

gnomAD v4: 1-152304926-A-C
MyVariant Identifiers: chr1:g.152277402A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304926A>C , CM000663.2:g.152304926A>C GRCh38
NC_000001.10:g.152277402A>C , CM000663.1:g.152277402A>C GRCh37
NC_000001.9:g.150544026A>C NCBI36
NG_016190.1:g.25278T>G , LRG_1028:g.25278T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.9960T>G MANE Select ENSP00000357789.1:p.Arg3320=
ENST00000368799.1:c.9960T>G ENSP00000357789.1:p.Arg3320=
NM_002016.1:c.9960T>G , LRG_1028t1:c.9960T>G NP_002007.1:p.Arg3320=
XM_011509329.1:c.9108+852T>G XP_011507631.1:n.9108+852T>G
NM_002016.2:c.9960T>G MANE Select NP_002007.1:p.Arg3320=
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