Canonical Allele Identifier: CA420927168
Gene: FLG HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.152277312T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304836T>G , CM000663.2:g.152304836T>G GRCh38
NC_000001.10:g.152277312T>G , CM000663.1:g.152277312T>G GRCh37
NC_000001.9:g.150543936T>G NCBI36
NG_016190.1:g.25368A>C , LRG_1028:g.25368A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.10050A>C MANE Select ENSP00000357789.1:p.Ser3350=
ENST00000368799.1:c.10050A>C ENSP00000357789.1:p.Ser3350=
NM_002016.1:c.10050A>C , LRG_1028t1:c.10050A>C NP_002007.1:p.Ser3350=
XM_011509329.1:c.9108+942A>C XP_011507631.1:n.9108+942A>C
NM_002016.2:c.10050A>C MANE Select NP_002007.1:p.Ser3350=