Canonical Allele Identifier: CA342089169

Gene: FLG

Linked Data

• dbSNP Id: rs1652508299
• MyVariant Identifiers: chr1:g.152284852C>A (hg19) ; chr1:g.152312376C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152312376C>A , CM000663.2:g.152312376C>A	GRCh38
NC_000001.10:g.152284852C>A , CM000663.1:g.152284852C>A	GRCh37
NC_000001.9:g.150551476C>A	NCBI36
NG_016190.1:g.17828G>T , LRG_1028:g.17828G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.2510G>T MANE Select	ENSP00000357789.1:p.Gly837Val
ENST00000368799.1:c.2510G>T	ENSP00000357789.1:p.Gly837Val
NM_002016.1:c.2510G>T , LRG_1028t1:c.2510G>T	NP_002007.1:p.Gly837Val
XM_011509329.1:c.2510G>T	XP_011507631.1:p.Gly837Val
NM_002016.2:c.2510G>T MANE Select	NP_002007.1:p.Gly837Val