Canonical Allele Identifier: CA1106019
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs769913812
ExAC: 1:152282480 G / C
gnomAD v2: 1-152282480-G-C
gnomAD v3: 1-152310004-G-C
gnomAD v4: 1-152310004-G-C
MyVariant Identifiers: chr1:g.152282480G>C (hg19) chr1:g.152310004G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152310004G>C , CM000663.2:g.152310004G>C GRCh38
NC_000001.10:g.152282480G>C , CM000663.1:g.152282480G>C GRCh37
NC_000001.9:g.150549104G>C NCBI36
NG_016190.1:g.20200C>G , LRG_1028:g.20200C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.4882C>G MANE Select ENSP00000357789.1:p.His1628Asp
ENST00000368799.1:c.4882C>G ENSP00000357789.1:p.His1628Asp
NM_002016.1:c.4882C>G , LRG_1028t1:c.4882C>G NP_002007.1:p.His1628Asp
XM_011509329.1:c.4882C>G XP_011507631.1:p.His1628Asp
NM_002016.2:c.4882C>G MANE Select NP_002007.1:p.His1628Asp
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