Canonical Allele Identifier: CA420926685
Gene: FLG HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.152277390T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304914T>G , CM000663.2:g.152304914T>G GRCh38
NC_000001.10:g.152277390T>G , CM000663.1:g.152277390T>G GRCh37
NC_000001.9:g.150544014T>G NCBI36
NG_016190.1:g.25290A>C , LRG_1028:g.25290A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.9972A>C MANE Select ENSP00000357789.1:p.Ser3324=
ENST00000368799.1:c.9972A>C ENSP00000357789.1:p.Ser3324=
NM_002016.1:c.9972A>C , LRG_1028t1:c.9972A>C NP_002007.1:p.Ser3324=
XM_011509329.1:c.9108+864A>C XP_011507631.1:n.9108+864A>C
NM_002016.2:c.9972A>C MANE Select NP_002007.1:p.Ser3324=
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