Canonical Allele Identifier: CA342072569
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs1570895283
gnomAD v4: 1-152304667-T-C
MyVariant Identifiers: chr1:g.152277143T>C (hg19) chr1:g.152304667T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304667T>C , CM000663.2:g.152304667T>C GRCh38
NC_000001.10:g.152277143T>C , CM000663.1:g.152277143T>C GRCh37
NC_000001.9:g.150543767T>C NCBI36
NG_016190.1:g.25537A>G , LRG_1028:g.25537A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000368799.2:c.10219A>G MANE Select ENSP00000357789.1:p.Thr3407Ala
ENST00000368799.1:c.10219A>G ENSP00000357789.1:p.Thr3407Ala
NM_002016.1:c.10219A>G , LRG_1028t1:c.10219A>G NP_002007.1:p.Thr3407Ala
XM_011509329.1:c.9109-834A>G XP_011507631.1:n.9109-834A>G
NM_002016.2:c.10219A>G MANE Select NP_002007.1:p.Thr3407Ala
Search 100 bp 5'
Search 100 bp 3'