Canonical Allele Identifier: CA420928849
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs1157533300
gnomAD v4: 1-152308772-C-A
MyVariant Identifiers: chr1:g.152281248C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152308772C>A , CM000663.2:g.152308772C>A GRCh38
NC_000001.10:g.152281248C>A , CM000663.1:g.152281248C>A GRCh37
NC_000001.9:g.150547872C>A NCBI36
NG_016190.1:g.21432G>T , LRG_1028:g.21432G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.6114G>T MANE Select ENSP00000357789.1:p.Gly2038=
ENST00000368799.1:c.6114G>T ENSP00000357789.1:p.Gly2038=
NM_002016.1:c.6114G>T , LRG_1028t1:c.6114G>T NP_002007.1:p.Gly2038=
XM_011509329.1:c.6114G>T XP_011507631.1:p.Gly2038=
NM_002016.2:c.6114G>T MANE Select NP_002007.1:p.Gly2038=
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