Canonical Allele Identifier: CA342055317

Gene: FLG

Linked Data

• dbSNP Id: rs774954937
• MyVariant Identifiers: chr1:g.152281151T>C (hg19) ; chr1:g.152308675T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.152308675T>C , CM000663.2:g.152308675T>C	GRCh38
NC_000001.10:g.152281151T>C , CM000663.1:g.152281151T>C	GRCh37
NC_000001.9:g.150547775T>C	NCBI36
NG_016190.1:g.21529A>G , LRG_1028:g.21529A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368799.2:c.6211A>G MANE Select	ENSP00000357789.1:p.Ser2071Gly
ENST00000368799.1:c.6211A>G	ENSP00000357789.1:p.Ser2071Gly
NM_002016.1:c.6211A>G , LRG_1028t1:c.6211A>G	NP_002007.1:p.Ser2071Gly
XM_011509329.1:c.6211A>G	XP_011507631.1:p.Ser2071Gly
NM_002016.2:c.6211A>G MANE Select	NP_002007.1:p.Ser2071Gly