Canonical Allele Identifier: CA342071140
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs1470787265

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152310031A>C , CM000663.2:g.152310031A>C GRCh38
NC_000001.10:g.152282507A>C , CM000663.1:g.152282507A>C GRCh37
NC_000001.9:g.150549131A>C NCBI36
NG_016190.1:g.20173T>G , LRG_1028:g.20173T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.4855T>G MANE Select ENSP00000357789.1:p.Tyr1619Asp
ENST00000368799.1:c.4855T>G ENSP00000357789.1:p.Tyr1619Asp
NM_002016.1:c.4855T>G , LRG_1028t1:c.4855T>G NP_002007.1:p.Tyr1619Asp
XM_011509329.1:c.4855T>G XP_011507631.1:p.Tyr1619Asp
NM_002016.2:c.4855T>G MANE Select NP_002007.1:p.Tyr1619Asp