Canonical Allele Identifier: CA420930876
Gene: FLG HGNC NCBI

Linked Data

gnomAD v3: 1-152311355-C-T
gnomAD v4: 1-152311355-C-T
MyVariant Identifiers: chr1:g.152283831C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152311355C>T , CM000663.2:g.152311355C>T GRCh38
NC_000001.10:g.152283831C>T , CM000663.1:g.152283831C>T GRCh37
NC_000001.9:g.150550455C>T NCBI36
NG_016190.1:g.18849G>A , LRG_1028:g.18849G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.3531G>A MANE Select ENSP00000357789.1:p.Gln1177=
ENST00000368799.1:c.3531G>A ENSP00000357789.1:p.Gln1177=
NM_002016.1:c.3531G>A , LRG_1028t1:c.3531G>A NP_002007.1:p.Gln1177=
XM_011509329.1:c.3531G>A XP_011507631.1:p.Gln1177=
NM_002016.2:c.3531G>A MANE Select NP_002007.1:p.Gln1177=
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