Canonical Allele Identifier: CA342080884
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs139456266
gnomAD v2: 1-152283533-C-A
gnomAD v4: 1-152311057-C-A
MyVariant Identifiers: chr1:g.152283533C>A (hg19) chr1:g.152311057C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152311057C>A , CM000663.2:g.152311057C>A GRCh38
NC_000001.10:g.152283533C>A , CM000663.1:g.152283533C>A GRCh37
NC_000001.9:g.150550157C>A NCBI36
NG_016190.1:g.19147G>T , LRG_1028:g.19147G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000368799.2:c.3829G>T MANE Select ENSP00000357789.1:p.Glu1277Ter
ENST00000368799.1:c.3829G>T ENSP00000357789.1:p.Glu1277Ter
NM_002016.1:c.3829G>T , LRG_1028t1:c.3829G>T NP_002007.1:p.Glu1277Ter
XM_011509329.1:c.3829G>T XP_011507631.1:p.Glu1277Ter
NM_002016.2:c.3829G>T MANE Select NP_002007.1:p.Glu1277Ter
Search 100 bp 5'
Search 100 bp 3'