Canonical Allele Identifier: CA420930471

Gene: FLG

Linked Data

• dbSNP Id: rs115324644
• gnomAD v2: 1-152283426-A-G
• gnomAD v4: 1-152310950-A-G
• MyVariant Identifiers: chr1:g.152283426A>G (hg19) ; chr1:g.152310950A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152310950A>G , CM000663.2:g.152310950A>G	GRCh38
NC_000001.10:g.152283426A>G , CM000663.1:g.152283426A>G	GRCh37
NC_000001.9:g.150550050A>G	NCBI36
NG_016190.1:g.19254T>C , LRG_1028:g.19254T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000368799.2:c.3936T>C MANE Select	ENSP00000357789.1:p.His1312=
ENST00000368799.1:c.3936T>C	ENSP00000357789.1:p.His1312=
NM_002016.1:c.3936T>C , LRG_1028t1:c.3936T>C	NP_002007.1:p.His1312=
XM_011509329.1:c.3936T>C	XP_011507631.1:p.His1312=
NM_002016.2:c.3936T>C MANE Select	NP_002007.1:p.His1312=