Canonical Allele Identifier: CA1103569

Gene: FLG

Linked Data

• dbSNP Id: rs760841920
• ExAC: 1:152277315 C / T
• gnomAD v2: 1-152277315-C-T
• gnomAD v4: 1-152304839-C-T
• MyVariant Identifiers: chr1:g.152277315C>T (hg19) ; chr1:g.152304839C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152304839C>T , CM000663.2:g.152304839C>T	GRCh38
NC_000001.10:g.152277315C>T , CM000663.1:g.152277315C>T	GRCh37
NC_000001.9:g.150543939C>T	NCBI36
NG_016190.1:g.25365G>A , LRG_1028:g.25365G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000368799.2:c.10047G>A MANE Select	ENSP00000357789.1:p.Glu3349=
ENST00000368799.1:c.10047G>A	ENSP00000357789.1:p.Glu3349=
NM_002016.1:c.10047G>A , LRG_1028t1:c.10047G>A	NP_002007.1:p.Glu3349=
XM_011509329.1:c.9108+939G>A	XP_011507631.1:n.9108+939G>A
NM_002016.2:c.10047G>A MANE Select	NP_002007.1:p.Glu3349=