Canonical Allele Identifier: CA342074723
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs145389873
gnomAD v2: 1-152277456-G-C
gnomAD v4: 1-152304980-G-C
MyVariant Identifiers: chr1:g.152277456G>C (hg19) chr1:g.152304980G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304980G>C , CM000663.2:g.152304980G>C GRCh38
NC_000001.10:g.152277456G>C , CM000663.1:g.152277456G>C GRCh37
NC_000001.9:g.150544080G>C NCBI36
NG_016190.1:g.25224C>G , LRG_1028:g.25224C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.9906C>G MANE Select ENSP00000357789.1:p.His3302Gln
ENST00000368799.1:c.9906C>G ENSP00000357789.1:p.His3302Gln
NM_002016.1:c.9906C>G , LRG_1028t1:c.9906C>G NP_002007.1:p.His3302Gln
XM_011509329.1:c.9108+798C>G XP_011507631.1:n.9108+798C>G
NM_002016.2:c.9906C>G MANE Select NP_002007.1:p.His3302Gln
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