Canonical Allele Identifier: CA342088045
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs1253823938
gnomAD v3: 1-152312249-C-A
gnomAD v4: 1-152312249-C-A
MyVariant Identifiers: chr1:g.152284725C>A (hg19) chr1:g.152312249C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152312249C>A , CM000663.2:g.152312249C>A GRCh38
NC_000001.10:g.152284725C>A , CM000663.1:g.152284725C>A GRCh37
NC_000001.9:g.150551349C>A NCBI36
NG_016190.1:g.17955G>T , LRG_1028:g.17955G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.2637G>T MANE Select ENSP00000357789.1:p.Arg879Ser
ENST00000368799.1:c.2637G>T ENSP00000357789.1:p.Arg879Ser
NM_002016.1:c.2637G>T , LRG_1028t1:c.2637G>T NP_002007.1:p.Arg879Ser
XM_011509329.1:c.2637G>T XP_011507631.1:p.Arg879Ser
NM_002016.2:c.2637G>T MANE Select NP_002007.1:p.Arg879Ser
Search 100 bp 5'
Search 100 bp 3'