Canonical Allele Identifier: CA30579237
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs2786680

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152325202A>T , CM000663.2:g.152325202A>T GRCh38
NC_000001.10:g.152297678A>T , CM000663.1:g.152297678A>T GRCh37
NC_000001.9:g.150564302A>T NCBI36
NG_016190.1:g.5002T>A , LRG_1028:g.5002T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000368799.2:c.-35T>A MANE Select ENSP00000357789.1:n.-35T>A
ENST00000368799.1:c.-35T>A ENSP00000357789.1:n.-35T>A
NM_002016.1:c.-35T>A , LRG_1028t1:c.-35T>A NP_002007.1:n.-35T>A
NR_103778.1:n.915-7381A>T
XM_011509329.1:c.-35T>A XP_011507631.1:n.-35T>A
NM_002016.2:c.-35T>A MANE Select NP_002007.1:n.-35T>A