Canonical Allele Identifier: CA420930446
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs1652366580
gnomAD v3: 1-152310923-G-A
gnomAD v4: 1-152310923-G-A
MyVariant Identifiers: chr1:g.152283399G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152310923G>A , CM000663.2:g.152310923G>A GRCh38
NC_000001.10:g.152283399G>A , CM000663.1:g.152283399G>A GRCh37
NC_000001.9:g.150550023G>A NCBI36
NG_016190.1:g.19281C>T , LRG_1028:g.19281C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.3963C>T MANE Select ENSP00000357789.1:p.His1321=
ENST00000368799.1:c.3963C>T ENSP00000357789.1:p.His1321=
NM_002016.1:c.3963C>T , LRG_1028t1:c.3963C>T NP_002007.1:p.His1321=
XM_011509329.1:c.3963C>T XP_011507631.1:p.His1321=
NM_002016.2:c.3963C>T MANE Select NP_002007.1:p.His1321=
Search 100 bp 5'
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