Canonical Allele Identifier: CA420931944

Gene: FLG

Linked Data

• dbSNP Id: rs775883344
• gnomAD v4: 1-152313890-G-C
• MyVariant Identifiers: chr1:g.152286366G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152313890G>C , CM000663.2:g.152313890G>C	GRCh38
NC_000001.10:g.152286366G>C , CM000663.1:g.152286366G>C	GRCh37
NC_000001.9:g.150552990G>C	NCBI36
NG_016190.1:g.16314C>G , LRG_1028:g.16314C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000368799.2:c.996C>G MANE Select	ENSP00000357789.1:p.Gly332=
ENST00000368799.1:c.996C>G	ENSP00000357789.1:p.Gly332=
NM_002016.1:c.996C>G , LRG_1028t1:c.996C>G	NP_002007.1:p.Gly332=
NR_103778.1:n.432G>C
XM_011509329.1:c.996C>G	XP_011507631.1:p.Gly332=
NM_002016.2:c.996C>G MANE Select	NP_002007.1:p.Gly332=