Canonical Allele Identifier: CA420931975
Gene: FLG HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.152286381C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152313905C>T , CM000663.2:g.152313905C>T GRCh38
NC_000001.10:g.152286381C>T , CM000663.1:g.152286381C>T GRCh37
NC_000001.9:g.150553005C>T NCBI36
NG_016190.1:g.16299G>A , LRG_1028:g.16299G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000368799.2:c.981G>A MANE Select ENSP00000357789.1:p.Glu327=
ENST00000368799.1:c.981G>A ENSP00000357789.1:p.Glu327=
NM_002016.1:c.981G>A , LRG_1028t1:c.981G>A NP_002007.1:p.Glu327=
NR_103778.1:n.447C>T
XM_011509329.1:c.981G>A XP_011507631.1:p.Glu327=
NM_002016.2:c.981G>A MANE Select NP_002007.1:p.Glu327=
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