Canonical Allele Identifier: CA342072115
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs768300379
gnomAD v4: 1-152310196-G-T
MyVariant Identifiers: chr1:g.152282672G>T (hg19) chr1:g.152310196G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152310196G>T , CM000663.2:g.152310196G>T GRCh38
NC_000001.10:g.152282672G>T , CM000663.1:g.152282672G>T GRCh37
NC_000001.9:g.150549296G>T NCBI36
NG_016190.1:g.20008C>A , LRG_1028:g.20008C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.4690C>A MANE Select ENSP00000357789.1:p.Pro1564Thr
ENST00000368799.1:c.4690C>A ENSP00000357789.1:p.Pro1564Thr
NM_002016.1:c.4690C>A , LRG_1028t1:c.4690C>A NP_002007.1:p.Pro1564Thr
XM_011509329.1:c.4690C>A XP_011507631.1:p.Pro1564Thr
NM_002016.2:c.4690C>A MANE Select NP_002007.1:p.Pro1564Thr
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