Canonical Allele Identifier: CA30551954
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs771395243
gnomAD v4: 1-152309181-T-C
MyVariant Identifiers: chr1:g.152281657T>C (hg19) chr1:g.152309181T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152309181T>C , CM000663.2:g.152309181T>C GRCh38
NC_000001.10:g.152281657T>C , CM000663.1:g.152281657T>C GRCh37
NC_000001.9:g.150548281T>C NCBI36
NG_016190.1:g.21023A>G , LRG_1028:g.21023A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.5705A>G MANE Select ENSP00000357789.1:p.Gln1902Arg
ENST00000368799.1:c.5705A>G ENSP00000357789.1:p.Gln1902Arg
NM_002016.1:c.5705A>G , LRG_1028t1:c.5705A>G NP_002007.1:p.Gln1902Arg
XM_011509329.1:c.5705A>G XP_011507631.1:p.Gln1902Arg
NM_002016.2:c.5705A>G MANE Select NP_002007.1:p.Gln1902Arg
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