Canonical Allele Identifier: CA30601979

Gene: FLG

Linked Data

• dbSNP Id: rs934375152
• MyVariant Identifiers: chr1:g.152277127C>T (hg19) ; chr1:g.152304651C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152304651C>T , CM000663.2:g.152304651C>T	GRCh38
NC_000001.10:g.152277127C>T , CM000663.1:g.152277127C>T	GRCh37
NC_000001.9:g.150543751C>T	NCBI36
NG_016190.1:g.25553G>A , LRG_1028:g.25553G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.10235G>A MANE Select	ENSP00000357789.1:p.Gly3412Glu
ENST00000368799.1:c.10235G>A	ENSP00000357789.1:p.Gly3412Glu
NM_002016.1:c.10235G>A , LRG_1028t1:c.10235G>A	NP_002007.1:p.Gly3412Glu
XM_011509329.1:c.9109-818G>A	XP_011507631.1:n.9109-818G>A
NM_002016.2:c.10235G>A MANE Select	NP_002007.1:p.Gly3412Glu