Canonical Allele Identifier: CA1103573
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs751449776
ExAC: 1:152277332 C / T
gnomAD v2: 1-152277332-C-T
gnomAD v4: 1-152304856-C-T
MyVariant Identifiers: chr1:g.152277332C>T (hg19) chr1:g.152304856C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304856C>T , CM000663.2:g.152304856C>T GRCh38
NC_000001.10:g.152277332C>T , CM000663.1:g.152277332C>T GRCh37
NC_000001.9:g.150543956C>T NCBI36
NG_016190.1:g.25348G>A , LRG_1028:g.25348G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.10030G>A MANE Select ENSP00000357789.1:p.Glu3344Lys
ENST00000368799.1:c.10030G>A ENSP00000357789.1:p.Glu3344Lys
NM_002016.1:c.10030G>A , LRG_1028t1:c.10030G>A NP_002007.1:p.Glu3344Lys
XM_011509329.1:c.9108+922G>A XP_011507631.1:n.9108+922G>A
NM_002016.2:c.10030G>A MANE Select NP_002007.1:p.Glu3344Lys
Search 100 bp 5'
Search 100 bp 3'