Canonical Allele Identifier: CA420930831
Gene: FLG HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.152284767T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152312291T>C , CM000663.2:g.152312291T>C GRCh38
NC_000001.10:g.152284767T>C , CM000663.1:g.152284767T>C GRCh37
NC_000001.9:g.150551391T>C NCBI36
NG_016190.1:g.17913A>G , LRG_1028:g.17913A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.2595A>G MANE Select ENSP00000357789.1:p.Gly865=
ENST00000368799.1:c.2595A>G ENSP00000357789.1:p.Gly865=
NM_002016.1:c.2595A>G , LRG_1028t1:c.2595A>G NP_002007.1:p.Gly865=
XM_011509329.1:c.2595A>G XP_011507631.1:p.Gly865=
NM_002016.2:c.2595A>G MANE Select NP_002007.1:p.Gly865=
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