Canonical Allele Identifier: CA420926963
Gene: FLG HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.152277249G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304773G>T , CM000663.2:g.152304773G>T GRCh38
NC_000001.10:g.152277249G>T , CM000663.1:g.152277249G>T GRCh37
NC_000001.9:g.150543873G>T NCBI36
NG_016190.1:g.25431C>A , LRG_1028:g.25431C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.10113C>A MANE Select ENSP00000357789.1:p.Ser3371=
ENST00000368799.1:c.10113C>A ENSP00000357789.1:p.Ser3371=
NM_002016.1:c.10113C>A , LRG_1028t1:c.10113C>A NP_002007.1:p.Ser3371=
XM_011509329.1:c.9109-940C>A XP_011507631.1:n.9109-940C>A
NM_002016.2:c.10113C>A MANE Select NP_002007.1:p.Ser3371=