Canonical Allele Identifier: CA342057347
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs1652166097
MyVariant Identifiers: chr1:g.152281217C>G (hg19) chr1:g.152308741C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152308741C>G , CM000663.2:g.152308741C>G GRCh38
NC_000001.10:g.152281217C>G , CM000663.1:g.152281217C>G GRCh37
NC_000001.9:g.150547841C>G NCBI36
NG_016190.1:g.21463G>C , LRG_1028:g.21463G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.6145G>C MANE Select ENSP00000357789.1:p.Gly2049Arg
ENST00000368799.1:c.6145G>C ENSP00000357789.1:p.Gly2049Arg
NM_002016.1:c.6145G>C , LRG_1028t1:c.6145G>C NP_002007.1:p.Gly2049Arg
XM_011509329.1:c.6145G>C XP_011507631.1:p.Gly2049Arg
NM_002016.2:c.6145G>C MANE Select NP_002007.1:p.Gly2049Arg
Search 100 bp 5'
Search 100 bp 3'