Canonical Allele Identifier: CA420930199

Gene: FLG

Linked Data

• dbSNP Id: rs1652387325
• gnomAD v4: 1-152311130-C-G
• MyVariant Identifiers: chr1:g.152283606C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152311130C>G , CM000663.2:g.152311130C>G	GRCh38
NC_000001.10:g.152283606C>G , CM000663.1:g.152283606C>G	GRCh37
NC_000001.9:g.150550230C>G	NCBI36
NG_016190.1:g.19074G>C , LRG_1028:g.19074G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.3756G>C MANE Select	ENSP00000357789.1:p.Val1252=
ENST00000368799.1:c.3756G>C	ENSP00000357789.1:p.Val1252=
NM_002016.1:c.3756G>C , LRG_1028t1:c.3756G>C	NP_002007.1:p.Val1252=
XM_011509329.1:c.3756G>C	XP_011507631.1:p.Val1252=
NM_002016.2:c.3756G>C MANE Select	NP_002007.1:p.Val1252=