Canonical Allele Identifier: CA420930931

Gene: FLG

Linked Data

• dbSNP Id: rs1299296242
• MyVariant Identifiers: chr1:g.152285070G>T (hg19) ; chr1:g.152312594G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152312594G>T , CM000663.2:g.152312594G>T	GRCh38
NC_000001.10:g.152285070G>T , CM000663.1:g.152285070G>T	GRCh37
NC_000001.9:g.150551694G>T	NCBI36
NG_016190.1:g.17610C>A , LRG_1028:g.17610C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.2292C>A MANE Select	ENSP00000357789.1:p.Gly764=
ENST00000368799.1:c.2292C>A	ENSP00000357789.1:p.Gly764=
NM_002016.1:c.2292C>A , LRG_1028t1:c.2292C>A	NP_002007.1:p.Gly764=
XM_011509329.1:c.2292C>A	XP_011507631.1:p.Gly764=
NM_002016.2:c.2292C>A MANE Select	NP_002007.1:p.Gly764=