Canonical Allele Identifier: CA420926906

Gene: FLG

Linked Data

• dbSNP Id: rs1651816434
• MyVariant Identifiers: chr1:g.152277069C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152304593C>T , CM000663.2:g.152304593C>T	GRCh38
NC_000001.10:g.152277069C>T , CM000663.1:g.152277069C>T	GRCh37
NC_000001.9:g.150543693C>T	NCBI36
NG_016190.1:g.25611G>A , LRG_1028:g.25611G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.10293G>A MANE Select	ENSP00000357789.1:p.Gln3431=
ENST00000368799.1:c.10293G>A	ENSP00000357789.1:p.Gln3431=
NM_002016.1:c.10293G>A , LRG_1028t1:c.10293G>A	NP_002007.1:p.Gln3431=
XM_011509329.1:c.9109-760G>A	XP_011507631.1:n.9109-760G>A
NM_002016.2:c.10293G>A MANE Select	NP_002007.1:p.Gln3431=