Canonical Allele Identifier: CA1103537

Gene: FLG

Linked Data

• dbSNP Id: rs141599535
• ExAC: 1:152277249 G / C
• gnomAD v2: 1-152277249-G-C
• gnomAD v3: 1-152304773-G-C
• gnomAD v4: 1-152304773-G-C
• MyVariant Identifiers: chr1:g.152277249G>C (hg19) ; chr1:g.152304773G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152304773G>C , CM000663.2:g.152304773G>C	GRCh38
NC_000001.10:g.152277249G>C , CM000663.1:g.152277249G>C	GRCh37
NC_000001.9:g.150543873G>C	NCBI36
NG_016190.1:g.25431C>G , LRG_1028:g.25431C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.10113C>G MANE Select	ENSP00000357789.1:p.Ser3371=
ENST00000368799.1:c.10113C>G	ENSP00000357789.1:p.Ser3371=
NM_002016.1:c.10113C>G , LRG_1028t1:c.10113C>G	NP_002007.1:p.Ser3371=
XM_011509329.1:c.9109-940C>G	XP_011507631.1:n.9109-940C>G
NM_002016.2:c.10113C>G MANE Select	NP_002007.1:p.Ser3371=